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Method for preparing 2-chloro-6-fluorobenzaldehyde

A technology of fluorobenzaldehyde and fluorotoluene is applied in the field of preparation of 2-chloro-6-fluorobenzaldehyde, can solve the problems of complex reaction process, high cost, high risk and the like, and achieves good product quality, reduced risk, Yield-enhancing effect

Active Publication Date: 2012-08-01
江苏万隆化学有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Sulfuric acid is highly corrosive and dangerous, and its storage and operation have high requirements for containers and operators, and the containers required for the reaction require acid and corrosion resistance, which increases production costs
In addition, the existing reaction process for preparing 2-chloro-6-fluorobenzaldehyde is relatively complicated, with high cost and large pollution

Method used

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  • Method for preparing 2-chloro-6-fluorobenzaldehyde
  • Method for preparing 2-chloro-6-fluorobenzaldehyde
  • Method for preparing 2-chloro-6-fluorobenzaldehyde

Examples

Experimental program
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Embodiment 1

[0023] The concrete process that present embodiment prepares 2-chloro-6-fluorobenzaldehyde is as follows:

[0024] 1) add 250g 2-chloro-6-fluorotoluene and 0.5ml phosphorus trichloride in the 500ml four-necked glass reaction flask that reflux condenser, tail gas absorption device and thermometer are housed (add phosphorus trichloride in this step and can To improve product quality), chlorine gas is introduced under the condition of 180°C under the irradiation of a metal halide lamp.

[0025] 2) detect the content of 2-chloro-6-fluorobenzyl chloride in the reaction flask liquid phase with gas chromatography, when detecting that the content of 2-chloro-6-fluorochlorobenzyl is less than 0.5%, stop logical chlorine, simultaneously to reaction flask Nitrogen was introduced into the bottle to remove unreacted chlorine in the bottle.

[0026] 3) Add 0.5g of iron-based solid superacid SO to the liquid phase of the reaction flask 4 2- / Fe 3 o 4 , under the condition of 180 ° C, 37...

Embodiment 2

[0029] 1) Add 250g of 2-chloro-6-fluorotoluene to a 500ml four-necked glass reaction flask equipped with a reflux condenser, tail gas absorption device and thermometer, and feed chlorine gas under the irradiation of a metal halide lamp at 150°C.

[0030] 2) detect the content of 2-chloro-6-fluorobenzyl chloride in the reaction flask liquid phase with gas chromatography, when detecting that the content of 2-chloro-6-fluorochlorobenzyl is less than 0.5%, stop logical chlorine, simultaneously to reaction flask Nitrogen was introduced into the bottle to remove unreacted chlorine in the bottle.

[0031] 3) Add 1 g of iron-based solid superacid SO to the liquid phase of the reaction flask 4 2- / Fe 3 o 4 , under the condition of 150°C, 40g of water was slowly and uniformly dropped into the reaction bottle within 3 hours, and kept warm for 4 hours, and the conversion of 2-chloro-6-fluorodichlorobenzyl and 2-chloro-6-fluorotrichlorobenzyl was detected by gas chromatography Complete...

Embodiment 3

[0034] This embodiment is basically the same as Embodiment 2, the difference is: (1) in the 1st) step, the light temperature is 120°C; (2) in the 3rd) step, the temperature when dripping water is 120°C; The temperature during potassium carbonate aqueous solution is 80 ℃; The pH value of adjusting mixed solution is 10; The holding time is 4.2 hours;

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Abstract

The invention relates to a method for preparing 2-chloro-6-fluorobenzaldehyde, and belongs to the technical field of organic synthesis. The method for preparing 2-chloro-6-fluorobenzaldehyde comprises the following steps of: performing chlorination on 2-chloro-6-fluorotoluene under illumination to obtain 2-chloro-6-fluorobenzyl chloride, 2-chloro-6-difluorobenzyl chloride, and 2-chloro-6-trifluorobenzyl chloride; when the content of 2-chloro-6-fluorobenzyl chloride is less than 0.5 percent, adding ferric solid superacid, dripping water at the temperature of between 100 and 200 DEG C, and preserving heat for 4+ / -5 hours; and adding alkali liquor, stirring to ensure that a liquid phase is layered, and performing reduced pressure distillation or rectification and purification on an organic phase which is obtained after the liquid phase is layered to obtain 2-chloro-6-fluorobenzaldehyde.

Description

technical field [0001] The invention relates to a preparation method of 2-chloro-6-fluorobenzaldehyde, which belongs to the technical field of organic synthesis. Background technique [0002] 2-Chloro-6-fluorobenzaldehyde is an important intermediate in organic synthesis. In the pharmaceutical industry, 2-chloro-6-fluorobenzaldehyde is mainly used to produce flucloxacillin with good antibacterial properties. The replacement product has better curative effect; in the pesticide industry, 2-chloro-6-fluorobenzaldehyde is mainly used in the production of high-efficiency and low-toxicity fungicides, known as biomimetic pesticide intermediates. [0003] At present, the preparation of 2-chloro-6-fluorobenzaldehyde is to chlorinate 2-chloro-6-fluorotoluene in benzoyl peroxide or azobisisobutyronitrile as a free radical initiator to obtain 2-chloro-6-fluoro Dichlorobenzyl is then hydrolyzed in 85% sulfuric acid at 90°C to obtain 2-chloro-6-fluorobenzaldehyde with a content of 99% an...

Claims

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Application Information

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IPC IPC(8): C07C47/55C07C45/43C07C63/70C07C51/04
Inventor 吴勇才史丽娟
Owner 江苏万隆化学有限公司
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