阅读说明：本技术 1,1-二溴-2,2-双（氯甲基）环丙烷的合成方法 (Synthesis method of 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane ) 是由 王银 哈雷克瑞什南·科拉图尔·纳拉西姆汉·昆奇塔帕达姆 拉格海温德·拉奥·莫莎拉 赵振宇 徐 于 2019-09-25 设计创作，主要内容包括：本发明公开了1,1-二溴-2,2-双(氯甲基)环丙烷的合成方法,包括以下步骤：2-氨基-2-羟基甲基丙烷-1,3-二醇和二氯亚砜进行氯取代反应得到(1,3-二氯-2-(氯甲基)丙烷-2-基)氨基砜酮；(1,3-二氯-2-(氯甲基)丙烷-2-基)氨基砜酮通过浓硫酸水溶液进行水解得到1,3-二氯-2-氯甲基丙-2-胺硫酸盐；1,3-二氯-2-氯甲基丙-2-胺硫酸盐在碱性条件下进行解盐,并关环得到2,2-双(氯甲基)氮杂环丙烷；2,2-双(氯甲基)氮杂环丙烷与亚硝酸钠反应得到3-氯-2-氯甲基丙-1-烯；3-氯-2-氯甲基丙-1-烯与三溴甲烷在碱性条件下反应生成1,1-二溴-2,2-双(氯甲基)环丙烷。本发明制备方法简单,可进行放大生产。(The invention discloses a method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane, which comprises the following steps: performing chlorine substitution reaction on 2-amino-2-hydroxymethyl propane-1, 3-diol and thionyl chloride to obtain (1, 3-dichloro-2- (chloromethyl) propane-2-yl) aminosulfonone; hydrolyzing (1, 3-dichloro-2- (chloromethyl) propane-2-yl) aminosulfone ketone by concentrated sulfuric acid aqueous solution to obtain 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate; 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate is subjected to salt decomposition under an alkaline condition, and ring closure to obtain 2, 2-bis (chloromethyl) aziridine; reacting 2, 2-bis (chloromethyl) aziridine with sodium nitrite to obtain 3-chloro-2-chloromethylprop-1-ene; 3-chloro-2-chloromethylprop-1-ene reacts with tribromomethane under alkaline condition to generate 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane. The preparation method is simple and can be used for large-scale production.)

A method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane, which is characterized by comprising the following steps:

A. preparation of (1, 3-dichloro-2- (chloromethyl) propan-2-yl) aminosulfonone: performing chlorine substitution reaction on 2-amino-2-hydroxymethyl propane-1, 3-diol and thionyl chloride to obtain (1, 3-dichloro-2- (chloromethyl) propane-2-yl) aminosulfonone;

B. preparation of 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate: hydrolyzing (1, 3-dichloro-2- (chloromethyl) propane-2-yl) aminosulfone ketone by concentrated sulfuric acid aqueous solution to obtain 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate;

C. preparation of 2, 2-bis (chloromethyl) aziridine: 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate is subjected to salt decomposition under an alkaline condition, and ring closure to obtain 2, 2-bis (chloromethyl) aziridine;

D. preparation of 3-chloro-2-chloromethylprop-1-ene: reacting 2, 2-bis (chloromethyl) aziridine with sodium nitrite to obtain 3-chloro-2-chloromethylprop-1-ene;

e: preparation of 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane: 3-chloro-2-chloromethylprop-1-ene reacts with tribromomethane under alkaline condition to generate 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane.

2. The method of synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane according to claim 1, comprising the steps of:

A. preparation of (1, 3-dichloro-2- (chloromethyl) propan-2-yl) aminosulfonone: dissolving 2-amino-2-hydroxymethyl propane-1, 3-diol in an organic solvent, controlling the temperature at 20-40 ℃, adding thionyl chloride, cooling to 10-15 ℃, adding pyridine, reacting at room temperature for 2 hours, heating in a gradient manner to 105 ℃ and 110 ℃ for 10 hours, and obtaining an organic solution of (1, 3-dichloro-2- (chloromethyl) propane-2-yl) aminosulfonone after the reaction is finished;

B. preparation of 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate: adding water and concentrated sulfuric acid aqueous solution into the organic solution of (1, 3-dichloro-2- (chloromethyl) propane-2-yl) aminosulfonone obtained in the step A at the temperature of not more than 25 ℃; heating to 85-95 ℃ for reaction for 15-22 hours; cooling to room temperature after the reaction is finished, standing, separating out a toluene phase, extracting the water phase with methyl tert-butyl ether, and separating out an organic phase to obtain an aqueous solution of 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate;

C. preparation of 2, 2-bis (chloromethyl) aziridine: c, cooling the aqueous solution of the 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate obtained in the step B to 10 ℃, adding sodium hydroxide solid and sodium hydroxide aqueous solution at the temperature of 10-20 ℃, controlling the pH to be 9-10, and heating to 40-45 ℃ for reacting for 8 hours; obtaining the aqueous solution of 2, 2-bis (chloromethyl) aziridine after the reaction is finished;

D. preparation of 3-chloro-2-chloromethylprop-1-ene: c, cooling the aqueous solution of the 2, 2-bis (chloromethyl) aziridine obtained in the step C to 5-10 ℃, adding sodium nitrite and concentrated hydrochloric acid, heating to 45-50 ℃ for reaction for 5 hours, after the reaction is finished, heating to 95-110 ℃ in a gradient manner, distilling at normal pressure, separating liquid, taking out the lower layer, and performing reduced pressure rectification to obtain 3-chloro-2-chloromethylprop-1-ene;

e: preparation of 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane: d, dissolving the 3-chloro-2-chloromethylprop-1-ene, the pinacol and the phase transfer catalyst obtained in the step D in the bromoform, controlling the temperature to be 18-25 ℃, dropping sodium hydroxide and a halogenated salt water solution, and reacting for 50 hours; after the reaction is finished, adding water and toluene, filtering through a pad of diatomite, washing filter cakes, combining filtrates, separating liquid, collecting an organic phase, concentrating to a small volume, adding n-heptane, crystallizing at 0 ℃, and filtering to obtain the 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane.

3. The method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane according to claim 2, wherein the molar ratio of 2-amino-2-hydroxymethylpropane-1, 3-diol to thionyl chloride in step a is 1: 3.0-6.0, and the organic solvent is toluene.

4. The method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane according to claim 2, wherein the molar ratio of (1, 3-dichloro-2- (chloromethyl) propan-2-yl) aminosulfonone to concentrated sulfuric acid in step B is 1: 1.0-1.5, and the organic solvent is toluene.

5. The method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane according to claim 2, wherein the molar ratio of 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate, sodium hydroxide, and potassium carbonate in step C is 1: 2.0-4.0: 1.0-2.0.

6. The method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane according to claim 2, wherein the molar ratio of 2, 2-bis (chloromethyl) aziridine to sodium nitrite in step D is 1: 1.0-1.2.

7. The method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane according to claim 2, wherein the molar ratio of 3-chloro-2-chloromethylprop-1-ene to tribromomethane in step E is 1: 2.0-4.0, the molar ratio of 3-chloro-2-chloromethylprop-1-ene to the halogenated salt is 1: 0.5-2.0, the halogenated salt is selected from one or more of sodium fluoride, sodium chloride, sodium bromide, sodium iodide, potassium fluoride, potassium chloride, potassium bromide and potassium iodide, and the phase transfer catalyst is one or more of 15-crown-5, 18-crown-6 and dibenzo-18-crown-6.

8. The method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane according to claim 7, wherein the halogenated salt in the step E is potassium bromide, and the phase transfer catalyst is dibenzo-18-crown-6.

Technical Field

The invention relates to an organic synthesis method, in particular to a synthesis method of 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane.

Background

1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane is a core intermediate of bicyclic (1.1.1) pentan-1-amine, a clinical drug candidate. The shortage of dicyclo (1.1.1) pentan-1-amine is caused by the large amount of purchase on the market, and 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane is just the core intermediate for quickly synthesizing the dicyclo (1.1.1) pentan-1-amine. However, several existing schemes for synthesizing the core fragment 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane have the problems of low yield, difficult amplification and the like.

Lynchand k.m. and dailyw.p. (ref. j. org.chem.1995,60,4666) using pentaerythriol as a starting material, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane was prepared using the route shown in the following reaction scheme. The technological steps of the method relate to that the decarboxylation reaction temperature needs at least 210 ℃, the reaction temperature is high, the conditions are harsh, and the dibromo-carbene generated in the last step is very unstable in a sodium hydroxide solution, has extremely violent heat release, is easy to flush in amplification and causes uncontrollable conditions.

Disclosure of Invention

The invention aims to solve the technical problems of low yield, high cost and difficult amplification of the existing method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane, and aims to provide a method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane and solve the problems of low yield and harsh conditions of the existing method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane.

The invention is realized by the following technical scheme:

the synthesis method of the 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane comprises the following steps:

A. preparation of (1, 3-dichloro-2- (chloromethyl) propan-2-yl) aminosulfonone: performing chlorine substitution reaction on 2-amino-2-hydroxymethyl propane-1, 3-diol and thionyl chloride to obtain (1, 3-dichloro-2- (chloromethyl) propane-2-yl) aminosulfonone;

B. preparation of 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate: hydrolyzing (1, 3-dichloro-2- (chloromethyl) propane-2-yl) aminosulfone ketone by concentrated sulfuric acid aqueous solution to obtain 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate;

C. preparation of 2, 2-bis (chloromethyl) aziridine: 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate is subjected to salt decomposition under an alkaline condition, and ring closure to obtain 2, 2-bis (chloromethyl) aziridine;

D. preparation of 3-chloro-2-chloromethylprop-1-ene: reacting 2, 2-bis (chloromethyl) aziridine with sodium nitrite to obtain 3-chloro-2-chloromethylprop-1-ene;

e: preparation of 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane: 3-chloro-2-chloromethylprop-1-ene reacts with tribromomethane under alkaline condition to generate 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane.

The synthesis method of the 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane relates to a reaction formula as follows:

preferably, the method for synthesizing the 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane comprises the following specific steps:

step A, (synthesis of 1, 3-dichloro-2- (chloromethyl) propan-2-yl) aminosulfonone: dissolving 2-amino-2-hydroxymethyl propane-1, 3-diol in an organic solvent, controlling the temperature at 20-40 ℃, adding thionyl chloride, cooling to 10-15 ℃, adding pyridine, reacting at room temperature for 2 hours, and carrying out gradient heating to 105-110 ℃ for 10 hours; after the reaction is finished, obtaining an organic solution of (1, 3-dichloro-2- (chloromethyl) propane-2-yl) aminosulfonone;

step B, synthesis of 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate: adding water and concentrated sulfuric acid aqueous solution into the obtained organic solution of (1, 3-dichloro-2- (chloromethyl) propane-2-yl) aminosulfonone at the temperature of not more than 25 ℃; heating to 85-95 ℃ for reaction for 15-22 hours; cooling to room temperature after the reaction is finished, standing, separating out a toluene phase, extracting the water phase with methyl tert-butyl ether, and separating out an organic phase to obtain an aqueous solution of 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate;

step C, synthesis of 2, 2-bis (chloromethyl) aziridine: cooling the obtained aqueous solution of 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate to 10 ℃, adding sodium hydroxide solid and sodium hydroxide aqueous solution at the temperature of 10-20 ℃, controlling the pH to be 9-10, and heating to 40-45 ℃ for reacting for 8 hours; obtaining the aqueous solution of 2, 2-bis (chloromethyl) aziridine after the reaction is finished;

step D, synthesis of 3-chloro-2-chloromethyl propan-1-ene: cooling the aqueous solution of the 2, 2-bis (chloromethyl) aziridine to 5-10 ℃, adding sodium nitrite and concentrated hydrochloric acid, heating to 45-50 ℃ for reaction for 5 hours, after the reaction is finished, heating to 95-110 ℃ in a gradient manner, distilling at normal pressure, separating liquid, taking out the lower layer, and performing reduced pressure rectification to obtain 3-chloro-2-chloromethylprop-1-ene;

step E, synthesis of 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane: dissolving the obtained 3-chloro-2-chloromethylprop-1-ene, pinacol and a phase transfer catalyst in bromoform, dropping sodium hydroxide and a halogenated salt water solution at the temperature of 18-25 ℃, and reacting for 50 hours; after the reaction is finished, adding water and toluene, filtering through a pad of diatomite, washing filter cakes, combining filtrates, separating liquid, collecting an organic phase, concentrating to a small volume, adding n-heptane, crystallizing at 0 ℃, and filtering to obtain the 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane.

In the above method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane, the molar ratio of 2-amino-2-hydroxymethylpropane-1, 3-diol to thionyl chloride in step a is 1: 3.0 to 6.0, if the thionyl chloride is less than 3.0 equivalent, the raw material reaction is not completely carried out, and if the thionyl chloride exceeds 6.0 equivalent, a large amount of waste gas is generated in the reaction; the organic solvent is toluene.

Wherein, in the above method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane, the molar ratio of (1, 3-dichloro-2- (chloromethyl) propane-2-yl) aminosulfonone and concentrated sulfuric acid in step B is 1: 1.0-1.5, and the organic solvent is toluene.

Wherein, in the above method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane, the molar ratio of the 1, 3-dichloro-2-chloromethylpropan-2-amine sulfate to sodium hydroxide and potassium carbonate in step C is 1: 2.0-4.0: 1.0-2.0, and the pH is controlled to be 9-10.

Wherein, in the above method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane, the molar ratio of 2, 2-bis (chloromethyl) aziridine to sodium nitrite in step D is 1: 1.0-1.2.

Wherein, in the above method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane, the molar ratio of 3-chloro-2-chloromethylprop-1-ene to tribromomethane in step E is 1: 2.0-4.0, if the amount of tribromomethane is less than 2.0 equivalent, the reaction of raw materials is slow and incomplete, and if the amount of tribromomethane exceeds 4.0 equivalent, a large amount of waste solids are generated.

In the method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane, the molar ratio of the 3-chloro-2-chloromethylprop-1-ene to the halogenated salt in the step E is 1: 0.5-2.0, the halogenated salt is selected from sodium fluoride, sodium chloride, sodium bromide, sodium iodide, potassium fluoride, potassium chloride, potassium bromide or potassium iodide, preferably potassium bromide, if the potassium bromide is less than 0.5 equivalent, the reaction heat release is obvious, the purpose of controlling the temperature cannot be achieved, and if the potassium bromide exceeds 2.0 equivalents, the system is viscous, and the reaction rate is influenced; the potassium bromide needs to be dissolved in the sodium hydroxide aqueous solution to play a buffering role, the potassium bromide is added to ensure that heat generated in the process of generating the carbene through the reaction is stably released, the reaction is ensured to be reacted in a temperature range specified by process parameters, so that the amplification and material flushing are avoided, the reaction is changed into impurities, the reaction temperature is controlled, the purpose that the amplification failure is caused because the amplification temperature suddenly rises suddenly and cannot be controlled is avoided, and the safety is ensured.

Among them, in the above-mentioned method for synthesizing 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane, the phase transfer catalyst in the step E is selected from crown ether catalysts such as 15-crown-5, 18-crown-6, dibenzo-18-crown-6 and the like, and dibenzo-18-crown-6 is preferable.

The invention uses cheap and easily obtained 2-amino-2-hydroxymethyl propane-1, 3-diol as an initial raw material to obtain 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane through 5 steps of simple reaction. In the last step of carbene reaction, halogenated salt is added as buffer, so that the instant heat release is greatly reduced; meanwhile, pinacol and crown ether catalysts are adopted for catalytic reaction, so that the reaction rate is ensured, the reaction rate is increased, and the yield can be effectively increased; solves the problems of low yield and harsh conditions of the existing method for synthesizing the 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane. The preparation method provided by the invention has the advantages of convenient and safe process operation and high total yield, and most importantly, can be used for large-scale production.

Compared with the prior art, the invention has the following advantages and beneficial effects:

1. the synthesis method of the 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane uses cheap and easily-obtained 2-amino-2-hydroxymethyl propane-1, 3-diol as an initial raw material, obtains the 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane through 5 steps of simple reaction, has simple preparation method, and can carry out amplification production;

2. according to the synthesis method of the 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane, the halogenated salt is added as a buffer in the last step of carbene reaction, so that the instant heat release is greatly reduced, the reaction is ensured to react within the temperature range specified by the process parameters, the purposes of material flushing, reaction impurity changing, reaction temperature control, failure of amplification caused by sudden violent rise of the amplification temperature and safety guarantee are avoided;

3. the synthesis method of the 1, 1-dibromo-2, 2-bis (chloromethyl) cyclopropane adopts pinacol and crown ether catalyst for catalytic reaction, ensures the reaction rate, improves the reaction rate and can effectively improve the yield.

Drawings

The accompanying drawings, which are included to provide a further understanding of the embodiments of the invention and are incorporated in and constitute a part of this application, illustrate embodiment(s) of the invention and together with the description serve to explain the principles of the invention. In the drawings:

FIG. 1 is a schematic diagram of the reaction of the present invention.

Detailed Description

In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention is further described in detail below with reference to examples and accompanying drawings, and the exemplary embodiments and descriptions thereof are only used for explaining the present invention and are not meant to limit the present invention.