CN1059711A

CN1059711A - The synthetic method of optically active camphor

Info

Publication number: CN1059711A
Application number: CN 90107672
Authority: CN
Inventors: 李允隆; 陈庆之; 杨国丽; 曹舒林; 蔡晓军; 刘尧权; 曾梅珍
Original assignee: Guangzhou Institute of Chemistry of CAS
Current assignee: Guangzhou Chemical Co Ltd of CAS; Guangzhou Institute of Chemistry of CAS
Priority date: 1990-09-10
Filing date: 1990-09-10
Publication date: 1992-03-25
Anticipated expiration: 2005-09-10
Also published as: CN1030315C

Abstract

The invention belongs to the optically active camphor synthetic method.

The camphor that obtains with general camphor synthesis method is racemization, and in the existing method of preparation optically active camphor, the optical purity of products obtained therefrom is more more than the optical purity reduction of raw material, and needs to use chemical reagent.The invention provides and a kind ofly make the artificial camphor method of catalyzer with zinc-calcium, this method makes borneol carry out solvent-free gas phase decompression dehydrogenation in fixed bed, and temperature is 240-320 ℃, and pressure is 0-60mmHg, when the material air speed is 0.05-0.8 ^-1Optical purity conservation rate 〉=99% of gained camphor, camphor purity 〉=99%, dehydrogenation reaction selectivity 〉=99%, the recovery rate of camphor 〉=95%.

Description

The synthetic method of optically active camphor

The invention belongs to the optically active camphor synthesis method.

Camphor is in industry and extensive use is pharmaceutically arranged, and optically active camphor is commonly used for the raw material of synthesizing chiral compound recently.General artificial camphor is all set out by α-Pai Xi, goes on foot through isomerization, esterification, hydrolysis and dehydrogenation etc. four to make.[J.D.Roberts and M.C.Caserio，Basic Principles of Organic Chemistry，W.A.Benjamin，InC.，Se-cond Edition 1977，P1467]。Its reaction formula is as follows:

Also can obtain isocamphol with the isomerization product camphene direct hydration of α-Pai Xi, the further dehydrogenation of the latter prepares camphor [CN 851 04105].In the above method isocamphol dehydrogenation is to adopt ventilation breather to make catalyzer, and adds dimethylbenzene and carry out as solvent, and the camphor that obtains all is racemizations.Natural camphor is optically active, its dextrorotation and levorotatory be respectively+and 44 ° and about-44 ° (C=10 is in the ethanol).It is dextral that natural camphor mostly is, and left-handed product are less, and price is also expensive.

Document [rattan original meaning people, the cigarette loyalty too, Songyuan City's justice is controlled, Japanization association will, 1975, (2) P.366-368] have proposed in the presence of Monochloro Acetic Acid, with the hydration of catalyzing cation exchange resin α-Pai Xi, product prepares optically active camphor with copper-zinc catalytic dehydrogenation.But with the camphor of this method preparation, its optical purity is more more than the optical purity reduction of raw material, and will add organic solvent in dehydrogenation reaction.Patent [CN85102398] has successfully been synthesized optical activity borneol with optical activity turps, and this provides raw material sources comparatively easily for PREPARATION OF OPTICALLY ACTIVE CAMPHOR.

Main points of the present invention are: (1) is raw material with the optical activity borneol of the method preparation of patent [CN85102398] or the optical activity borneol in other source.(2) make catalyzer with zinc-calcium, make borneol gas phase decompression dehydrogenation in fixed bed prepare camphor.Need not solubilizing agent in the reaction, temperature of reaction is 240-320 ℃, and pressure is 0-50mmHg, when the material air speed is 0.05-0.8 ^-1

Dehydrogenation reaction is carried out in the fixed bed flow through reactors.This device mainly is made up of stock bottle, reaction column and susceptor.The reaction column apparatus with catalyst inside has heating system outward, and its lower end links to each other with the stock bottle that has three mouths.All the other two mouths of this bottle connect the hydrogen plenum system respectively and insert thermometer, the outer heating system that is provided with of bottle.The upper end of post links to each other with susceptor, and the latter is joined through condenser and vacuum system.Catalyzer must be used hydrogen reducing before use, carries out 2-6 hour under 250-340 ℃ of normal pressure.Catalyzer can be reused, and can regenerate behind active the decline.

Camphor optical purity conservation rate 〉=99% of the inventive method preparation, camphor purity 〉=99%, the selectivity of dehydrogenation reaction 〉=99%, the recovery rate of camphor 〉=95%.

Example one

By the method for right [CN85102398], be 98.7% with purity, (α) ²⁵ _D+ 47.00 ° α-Pai Xi is a raw material, prepares borneol with the dealuminium mordenite catalytic hydration.Product is handled with mordenite and is removed isocamphol, and obtaining purity is 99.6%, (α) ²⁵ _D+ 34.40 ° borneol is got its 30.6 gram and is put into stock bottle.Put 1101 type zinc-calcium catalysts 200 and restrain in reaction column, and 285 ℃ of following logical hydrogen reductions 4 hours.Stop logical hydrogen then, being evacuated to pressure is 15mmHg, keeps column temperature at 285 ℃, heating raw bottle to 120 ℃.After 2 hours, obtain camphor 29.1 grams, purity is 100%, (α) ²⁵ _D+ 40.88 °, yield is 96.4%.

Example two

With purity is 99.5%, (α) ²⁵ _D+ 32.40 ° borneol 30.0 grams are raw material, press example 1 operation, and the control column temperature is at 290 ℃, and raw material and temperature are at 135 ℃, and pressure is 20mmHg.Through obtaining camphor 28.3 grams after the reaction in 45 minutes, purity is 100%, (α) ²⁵ _D+ 38.50 °, yield is 95.6%.

Example three

Is 98.6% by example 1 operation with purity, (α) ²⁵ _D-24.10 ° α-Pai Xi is a raw material, and making purity is 99.7%, (α) ²⁵ _D-18.10 ° borneol.Get its 15 gram and be dehydrogenation feed, the control column temperature is at 290 ℃, and the stock bottle temperature is at 120 ℃, and pressure is 15mmHg, after reaction in 1 hour, obtains camphor 14.2 grams.Its purity is 100%, (α) ²⁵ _D-21.50 °, yield is 96.0%.

Example four

With purity is 99.5%, (α) ²⁵ _D-30.50 ° borneol 35 grams are raw material.Press example 1 operation, control column temperature at 280 ℃, 125 ℃ of stock bottle temperature, pressure is 20mmHg.Obtain camphor 33.7 grams after reaction in 2 hours, purity is 100%, (α) ²⁵ _D-36.25 °, yield 97.6%.

Claims

1, a kind of method for preparing optically active camphor, this method is carried out dehydrogenation reaction with optical activity borneol, it is characterized by dehydrogenation reaction and carries out under the gas phase decompression, must not add any solvent, temperature of reaction is 240-320 ℃, and pressure is 0-60mmHg, when the material air speed is 0.05-0.8 ^-1, whole process is finished in the fixed bed flow through reactors.

2,, it is characterized in that described fixed bed is zinc-calcium type solid catalyst according to the method described in the claim 1.

3, according to the method described in the claim 1, it is characterized in that described fixed bed flow through reactors, form by stock bottle, reaction column and susceptor, catalyzer is housed in the reaction column, heating system is arranged outward, and the one end links to each other with stock bottle, and the other end links to each other with vacuum system through susceptor, condenser, stock bottle links to each other with hydrogen gas system, and heating system is arranged.

4, according to claim 1,2 described methods, its feature must be through hydrogen reducing before described catalyzer uses, and reduction temperature is 250-340 ℃, time 2-6 hour, the use of can regenerating after the catalyst activity reduction.