Production method for preparing chlorinated aniline via chlorination of nitrobenzene hydrogenation by utilizing solvent-free process

A technology of chloronitrobenzene and chloroaniline, applied in the field of solvent-free hydrogenation of chloronitrobenzene to prepare chloroaniline, which can solve the problems of unsafe use of Raney-Ni, product solvent loss, and product purity decline , to achieve low cost, reduce environmental pressure, and reduce equipment investment

Inactive Publication Date: 2013-05-22
SHANDONG FUYUAN CHEM
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the catalytic hydrogenation process of chloroaniline has the problem of hydrogenolysis and dechlorination, which causes equipment corrosion and product purity decline. Choosing the right additive can effectively reduce dechlorination and increase the content of the main product. Key points and difficulties of research in this field
Most of the traditional processes use Raney n...

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0018] Add 400 g of o-chloronitrobenzene and 3 grams of 1% Pt / C noble metal catalyst (self-made) into a 1L autoclave, close the autoclave, open the hydrogen valve, feed hydrogen into the autoclave, stir and heat up the reaction, the reaction temperature Control 80-100°C, control the reaction pressure 0.3-2.5MPA, set the reaction speed at 700 rpm, react until no hydrogen is absorbed, close the hydrogen valve, open the autoclave after cooling, discharge, filter and add to the separatory funnel , Separate the water generated by the reaction, the oil phase is o-chloroaniline, the purity of the gas chromatography analysis is 97.22%, the dechlorination amount is 1.9%, and the pH value of the oil phase is between 4-5.

Embodiment 2

[0020] Add 400 g of o-chloronitrobenzene, 3 grams of 1% Pt / C noble metal catalyst (self-made), and 0.7 grams of ethanolamine into a 1L autoclave, close the autoclave, open the hydrogen valve, feed hydrogen into the autoclave, and stir to raise the temperature Reaction, the reaction temperature is controlled at 80-100°C, the reaction pressure is controlled at 0.3-2.5MPA, the reaction speed is set at 700 rpm, the reaction is until no hydrogen is absorbed, the hydrogen valve is closed, the autoclave is opened after cooling, the material is discharged, filtered and then added In the separatory funnel, separate the water generated by the reaction, the oil phase is o-chloroaniline, the purity is 98.87% by gas chromatography, the dechlorination amount is 0.7%, and the pH value of the oil phase is between 5-6.

Embodiment 3

[0022] Add 400 g of o-chloronitrobenzene, 3 grams of 1% Pt / C noble metal catalyst (self-made), and 2 ml of pyridine into a 1L autoclave, close the autoclave, open the hydrogen valve, feed hydrogen into the autoclave, stir and heat up the reaction , the reaction temperature is controlled at 80-100°C, the reaction pressure is controlled at 0.3-2.5MPA, the reaction speed is set at 700 rpm, and the hydrogen gas valve is closed until the hydrogen is not absorbed. After cooling, the autoclave is opened, and the material is discharged. In the liquid funnel, the water generated by the reaction was separated, and the oil phase was o-chloroaniline, the purity of which was analyzed by gas chromatography was 98.72%, the dechlorination amount was 0.9%, and the pH value of the oil phase was between 5-6.

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PUM

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Abstract

The invention belongs to the production field of catalytic hydrogenation, and particularly discloses a production method for preparing chlorinated aniline via the chlorination of nitrobenzene hydrogenation by utilizing a solvent-free process. Chlorinated nitrobenzene is used as a raw material. The method is characterized in that under the existence of a catalyst and an aiding agent, the chlorinated nitrobenzene reacts with hydrogen at the temperature of 80 to 100 DEG C and under the pressure of 0.3 to 2.5 MPa, wherein a solvent is not added; and after the reaction is finished, the water diversion treatment is carried out, thereby obtaining the chlorinated aniline. The catalyst containing 1% of Pt/C precious metal is developed independently, wherein the adding amount of the catalyst accounts for 0.05% to 20% of that of the chlorinated nitrobenzene as the raw material. The aiding agent is a mixture of ethanol amine and pyridine, wherein the adding amount of the aiding agent accounts for 0.01% to 10% of that of the chlorinated nitrobenzene as the raw material. For the obtained o-chloroaniline, the chromatographic purity is above 99.5%, and the dechlorination quantity can be controlled within 0.1%. For the obtained 2,5-dichloroaniline, the chromatographic purity is above 99%, and the dechlorination quantity can be controlled within 0.1%. For the obtained 3,4-dichloroaniline, the chromatographic purity is above 99%, and the dechlorination quantity can be controlled within 0.1%.

Description

technical field [0001] The invention belongs to the field of catalytic hydrogenation production, and particularly discloses a production method for preparing chloroaniline by hydrogenation of chlorinated nitrobenzene in a solventless method. Background technique [0002] Chloroaniline is an important class of fine chemical intermediates, and has a wide range of uses in the fields of medicine, pesticides, dyes and daily chemicals. O-chloroaniline is the color base of ice dyes, and can also be used as the diazo component of azo dyes to produce acid black, acid blue and organic lakes such as permanent yellow R, permanent red FR, Hansa yellow HR, etc. It can also be used to prepare medicines, pesticides, and cross-linking agent methyl dichloroaniline of polyurethane resin; 2, 5-dichloroaniline is an important intermediate of medicines and pesticides, mainly used to synthesize the pesticide dicamba, and can also be used to make ice Dye dye bright red base and nitrogen fertilizer...

Claims

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Application Information

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IPC IPC(8): C07C211/52C07C209/36
Inventor 张红艳王超王其军司立朋陈娟
Owner SHANDONG FUYUAN CHEM
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