Synthetic method of 2-(trimethylsilyl)ethoxymethyl chloride

A technology of ethoxymethyl chloride and a synthetic method, which is applied in the synthesis field of 2-ethoxymethyl chloride, can solve the problems of violent reaction, low purity, instability, etc., and achieves improved yield, improved reaction efficiency, and improved stability. Sex-enhancing effects

Active Publication Date: 2018-08-17
兰州紫东药业有限公司
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  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, there will still be water production during the first step of the reaction, which will destroy the intermediate, generate impurities, and reduce the yield.
In the second step of replacement, when butyllithium is used alone, the alkalinity is too strong, and there will be a large amount of impurities replaced by chlorine, which will seriously affect the yield and purity of the product.
The reaction is violent, it is difficult to control, and the cost of lithium aluminum hydride is very high, the operation is dangerous, and the post-processing is difficult
The entire cost of this process is very high, and the reaction is dangerous and difficult to control, so it has been abandoned abroad
The raw material chloromethyltrimethylsilane used in the second method is expensive and the cost is higher
However, the product is unstable under acidic conditions, so that the total yield of the product prepared by this process is not high, the purity is not high, and it is not easy to store

Method used

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  • Synthetic method of 2-(trimethylsilyl)ethoxymethyl chloride
  • Synthetic method of 2-(trimethylsilyl)ethoxymethyl chloride
  • Synthetic method of 2-(trimethylsilyl)ethoxymethyl chloride

Examples

Experimental program
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Effect test

Embodiment 1

[0044] The first step of chloromethylation: Take 5L of n-hexane, 5kg of bromoethanol, 1300g of paraformaldehyde, and 800g of concentrated sulfuric acid, put them into a 20L reaction bottle, and start stirring. The system was cooled to -5-0°C, and HCL gas was introduced. Introduce slowly at the beginning, and after about 10 minutes, speed up the aeration rate and control the internal temperature to 5-8°C. When the reaction solution becomes clear, slow down the aeration rate again. Gas phase monitoring, until the raw material is less than 5%, stop ventilation (about 2450g of shared hydrogen chloride). Add 10 g of stabilizer to the reaction liquid, and stir for 5 min. The layers were separated, and the lower layer was extracted once with 2 L of n-hexane, and the organic phases were combined. Concentrate under reduced pressure at 50°C (recovery of n-hexane is applied mechanically), until there are no bubbles and no reflux to obtain a crude product. 60-90°C, water pump rectifica...

Embodiment 2

[0048] The first step of chloromethylation: Take 5L of n-hexane, 5kg of bromoethanol, 1300g of paraformaldehyde, and 800g of concentrated sulfuric acid, put them into a 20L reaction bottle, and start stirring. The system was cooled to -5-0°C, and HCL gas was introduced. Introduce slowly at the beginning, and after about 10 minutes, speed up the aeration rate and control the internal temperature to 5-8°C. When the reaction solution becomes clear, slow down the aeration rate again. Gas phase monitoring, until the raw material is less than 5%, stop ventilation (about 2490g of shared hydrogen chloride). Add 10 g of stabilizer to the reaction liquid, and stir for 5 min. The layers were separated, and the lower layer was extracted once with 2 L of n-hexane, and the organic phases were combined. Concentrate under reduced pressure at 50°C (recovery of n-hexane is applied mechanically), until there are no bubbles and no reflux to obtain a crude product. 60-90°C, water pump rectifica...

Embodiment 3

[0052] The first step of chloromethylation: Take 10L of n-hexane, 10kg of bromoethanol, 2600g of paraformaldehyde, and 1600g of concentrated sulfuric acid, put them into a 50L reaction kettle, and start stirring. The system was cooled to -5-0°C, and HCL gas was introduced. Introduce slowly at the beginning, and after about 10 minutes, speed up the aeration rate and control the internal temperature to 5-8°C. When the reaction solution becomes clear, slow down the aeration rate again. Gas phase monitoring, until the raw material is less than 5%, stop ventilation (about 5080g of shared hydrogen chloride). Add 25 g of stabilizer to the reaction liquid, and stir for 5 min. The layers were separated, and the lower layer was extracted once with 4 L of n-hexane, and the organic phases were combined. Concentrate under reduced pressure at 50°C (recovery of n-hexane is applied mechanically), until there are no bubbles and no reflux to obtain a crude product. 60-90°C, water pump rectif...

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Abstract

The invention provides a synthetic method of 2-(trimethylsilyl)ethoxymethyl chloride, comprising the steps: (1) allowing chloromethylation, to be specific, adding bromoethanol, n-hexane, paraformaldehyde, and concentrated sulfuric acid into a reaction bottle, starting stirring, cooling the temperature to -5-DEG C, introducing HCL gas until the raw material is less than 5%, stopping gas introduction, and performing reacting to obtain a chloromethylation intermediate; (2) carrying out substitution, to be specific, taking tetrahydrofuran, adding into the reaction bottle, opening, stirring, cooling to 15 DEG C, taking butylmagnesium chloride and n-butyllithium sequentially, adding into a reaction liquid, maintaining the inner temperature to 25 DEG and below, holding the temperature at 20-25 DEG C, stirring, dropwise adding the chloromethylation intermediate of step (1) slowly into the reaction liquid, holding the temperature to 30 DEG C and below, holding the temperature to 20-30 DEG C forreaction, concentrating the reaction liquid under reduced pressure, recycling organic solvents and the crude product, and distilling via a crude water pump. The synthetic method is low in cost, highin yield and good in post-treatment convenience and stability.

Description

Technical field: [0001] The invention relates to a synthesis method of 2-(trimethylsilyl)ethoxymethyl chloride, which belongs to the technical field of pharmacy. Background technique: [0002] 2-(Trimethylsilyl)ethoxymethyl chloride (SEM-Cl), as a commonly used organosilicon protective agent, is favored for its functional selectivity, and is an important intermediate in organic synthesis. It is used in the synthesis of medicine, biology and pesticides all play an important role. However, it is expensive, not easy to store, and not high in purity. It has always been the concern of producers and users, and it is a problem that needs to be solved urgently. [0003] The scheme commonly adopted in the prior art is relatively single, and the key intermediate of the product, trimethylsilyl alcohol, is used as the main intermediate, and the final product is obtained through chloromethylation. Trimethylsilyl ethanol has the following synthetic methods: [0004] (1) Using ethyl 2-b...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07F7/08
CPCC07F7/0827
Inventor 崔家乙伍有本艾杨保
Owner 兰州紫东药业有限公司
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