Synthesis method of isoflurane

A synthetic method, the technology of isoflurane, which is applied in the field of medicine and chemical industry, can solve the problems of low conversion rate of ether compounds, increase of by-products, low conversion rate, etc., and achieve the effect of improving purity, reducing the generation of by-products, and improving conversion rate

Active Publication Date: 2010-09-15
SHANDONG INST OF PHARMA IND
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Problems solved by technology

[0018] 2. In the chlorination process of the etherified compound, the etherified compound needs to be dried, and a large amount of hydrogen chloride gas is generated after the reaction of chlorine gas, and the escape of the hydrogen chloride gas has a strong effect of carrying material, which requires a cryogenic cold trap for cooling and reflux ( The boiling point of the ether compound is only 29.5°C), which requires a lot of cooling power to be wasted in production
[0019] 3. In order to reduce the formation of by-products in the chlorination process, the molar ratio of ether compounds and chlorine is usually low, about 1:0.3, that is, the conversion rate is low during each chlorination, and too much chlorine will make by-products The product increases significantly, which not only reduces the yield, but also increases the difficulty of separation
[0020] 4. Since the selectivity of the three hydrogen atoms in th

Method used

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  • Synthesis method of isoflurane
  • Synthesis method of isoflurane
  • Synthesis method of isoflurane

Examples

Experimental program
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Effect test

Embodiment 1

[0049] Example 1: Chlorination of (2,2,2-trifluoroethyl)-difluoromethyl ether

[0050] Add 450g of ether compound and 60ml of water into a four-neck flask equipped with an ice-salt condenser, a thermometer, a mechanical stirrer and an air inlet duct, start the stirrer, first pass nitrogen gas for 3-5min, and discharge the oxygen in it, and then Chlorine gas is passed down. The water bath controls the reaction temperature at 5-15° C. When about 40 liters (about 1.8 mol) of chlorine gas is fed in, the chlorine gas flow is stopped, and the stirring reaction is continued for 30 minutes.

[0051] The reaction solution was transferred to a separatory funnel for layering, and the organic layer solution was washed once with ice-cold 10% (w / w) sodium hydroxide aqueous solution, then washed with cold water until neutral, and dried with anhydrous calcium chloride.

[0052] Put the above dried mixed solution into a rectification bottle, install a high-efficiency fractionation column for ...

Embodiment 2

[0053] Example 2: Reduction of (1,1-dichloro-2,2,2-trifluoroethyl)-difluoromethyl ether

[0054] Add 20ml of isopropanol to the residue after rectification in Example 1, control the temperature at 20-30°C, and light for 2 hours under the protection of stirring and nitrogen flow, distill the reactant, and collect the fraction at 60-68°C. Isoflurane and acetone azeotrope 19.6g.

Embodiment 3

[0055] Example 3: Chlorination of (2,2,2-trifluoroethyl)-difluoromethyl ether

[0056] Adopt the method similar to embodiment 1, difference is to increase the consumption of water, promptly replaces 60ml water with 80ml water. 177g of etherified compound and 262g of crude isoflurane were recovered, and the remaining high-fraction substance was reduced by adding isopropanol.

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Abstract

The invention discloses a synthesis method of (1-chloro-2,2,2-trifluoroethyl)-difluoromethyl ether (isoflurane, whose structure is as the right figure), belonging to the field of pharmaceutical chemicals. The method takes (2,2,2-trifluoroethyl)-difluoromethyl ether (etherate) as starting material and comprises the following steps of: adding a right amount of water to the etherate; introducing chlorine for chlorination to obtain a mixture of isoflurane, a few impurities and unreacted etherate; carrying out fractionation to obtain the crude isoflurane; reducing the main impurity (1,1-dichloro-2,2,2-trifluoroethyl)-difluoromethyl ether by isopropanol under the sun light to obtain the azeotrope of the isoflurane and the acetone again; combining the collected crude isoflurane and the azeotrope; adding the acetone and carrying out distillation purification to obtain the isoflurane. The method has easy quality control, high yield, low cost and safe and convenient operation and is suitable for industrial production.

Description

technical field [0001] The invention relates to a synthesis method of organic compounds, in particular to a synthesis method of (1-chloro-2,2,2-trifluoroethyl)-difluoromethyl ether, belonging to the field of medicine and chemical industry. Background technique [0002] Isoflurane is an inhaled general anesthetic and is the isomer of enflurane. Isoflurane is a colorless, transparent liquid with a special fragrance. The blood / air distribution coefficient is small, the anesthesia induction is stable, rapid and comfortable, the recovery is fast, the muscles relax well, and there is no excitatory effect on the sympathetic nervous system. Occasional nausea and vomiting, is currently commonly used clinical inhalation anesthetics. [0003] The synthetic method bibliographical report of isoflurane is more, and U.S. Patent US3535425 (1970) has reported following synthetic method, obtains corresponding methyl ether with trifluoroethanol and dimethyl sulfate reaction under basic condi...

Claims

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Application Information

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IPC IPC(8): C07C43/12C07C41/22C07C41/24
Inventor 段崇刚陈广岭张雯
Owner SHANDONG INST OF PHARMA IND
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