Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Process for producing benzyl chlorides chemical compound

A compound and material technology applied in the production of benzyl chloride compounds, which can solve the problems of product coking, high temperature heat source, high energy consumption, etc., and achieve the effects of reaction operation control, high economic benefits, and easy reaction operation

Active Publication Date: 2007-11-14
NANJING UNIV OF TECH
View PDF0 Cites 17 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] The selectivity of benzyl chloride compounds can be improved by adopting chlorination rectification technology, but the integration of chlorination reaction and rectification in a tower equipment has the following defects: (1) the size of the reaction space is limited by the rectification tower structure
For the gas-liquid heterogeneous reaction of toluene chlorination, it is necessary to provide enough reaction space to keep the liquid holdup as large as possible. The liquid holdup of the packed tower itself is relatively small, which is difficult to meet the needs of large-scale production.
If a plate tower is used, the reaction section needs to have a larger tower diameter and a higher overflow weir than the rectification section, which will inevitably cause inconsistencies in the equipment size and fluid mechanical properties of the reaction zone and the rectification zone, which will increase the design and complexity of the rectification column. Difficulty in stable operation
(2) Benzyl chloride compounds are often produced by photocatalytic chlorination, and it is difficult to provide light to the reaction area in the reactive distillation tower
The suitable operating conditions for the side chain chlorination of methylbenzene compounds are normal pressure and temperature at 95-105°C, while the boiling points of the chlorinated target products benzyl chloride, o-chlorobenzyl chloride, and p-chlorobenzyl chloride are 179.4°C, respectively. , 217°C and 222°C, if the normal pressure operation is adopted, the reactive distillation requires a high temperature heat source and high energy consumption, and the long-term cooking of the product at high temperature will also cause problems such as coking

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Process for producing benzyl chlorides chemical compound

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] Toluene and chlorine feed are both 1.40kmol / h, the distribution ratio of chlorine in the three reactors is: 0.45:0.32:0.23, the amount of condensation at the top of the tower: 1000L / h, the temperature of the chlorination reactor is 105°C, rectification The operating pressure of the tower is 0.025MPa, the number of trays in the rectification zone is 9, and the number of trays in the separation zone is 30. After reactive distillation, the molar composition of the material in the tower kettle is: 0.48% toluene, 99.25% benzyl chloride, 0.26% benzylidene dichloride, and 0.04% cyclochlorotoluene. The selectivity of benzyl chloride is 98.96%.

Embodiment 2

[0022] Both toluene and chlorine feed are 1.40 kmol / h, the distribution ratio of chlorine in the three reactors is: 0.45:0.32:0.23, and the condensation at the top of the tower is 1300 L / h. , the temperature of the chlorination reactor is 80°C, the operating pressure of the rectification tower is 0.01MPa, the number of trays in the rectification zone is 6, and the number of trays in the separation zone is 26. After reactive distillation, the molar composition of the material in the tower kettle is: 0.46% toluene, 99.29% benzyl chloride, 0.21% benzylidene dichloride, and 0.04% cyclochlorotoluene. The selectivity of benzyl chloride is 99.08%.

Embodiment 3

[0024]Both p-chlorotoluene and chlorine feed are 1.40 kmol / h, the distribution ratio of chlorine in the four reactors is: 0.38:0.28:0.20:0.18, the amount of condensation at the top of the tower: 1000L / h, and the temperature of the chlorination reactor is 105 °C, the operating pressure of the rectification tower is 0.004MPa, the number of trays in the rectification zone is 8, and the number of trays in the separation zone is 30. After reactive distillation, the molar composition of the material in the tower kettle is: p-chlorotoluene 0.43%, p-chlorobenzyl chloride 99.07%, p-chlorobenzylidene dichloride 0.48%, cyclodichlorotoluene 0.02%. The selectivity to chlorobenzyl chloride is 98.59%.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
boiling pointaaaaaaaaaa
Login to View More

Abstract

This invention relates to a method of producing benzyl chloride compound. First according to a certain mol ratio series inlet methyl benzene compounds and chlorine to reactor that coupled with fractionating tower, after reaction the material enter rectify section, then enter next order reactor to take chlorination reaction; under series stable operation condition, control the operating pressure of fractionating tower at 0.002 to 0.1 MPa. The chlorination is stimulated by sunlight or blue light, temperature of reactor is controlled at 80 to 120 deg. The mole fraction of benzyl chloride or chlor-benzyl chloride that series discharged from tower kettle could reach 99%upwards, manufacturing cost is low, and economic benefit high.

Description

technical field [0001] The invention relates to a method for producing benzyl chloride compounds, specifically, toluene or chlorotoluene is directly chlorinated with chlorine to generate benzyl chloride or chlorobenzyl by using a method coupled with a reactor and a rectification tower Chlorine method. Background technique [0002] Benzyl chloride, also known as benzyl chloride or phenylmethane, is an important organochlorine intermediate widely used in pesticides, medicines, spices, plastic additives, surfactants, etc., and can be used to produce benzyl alcohol, benzaldehyde, Phenylacetonitrile, phenylacetic acid, benzyl butylamine, butyl benzyl phthalate, benzyl quaternary ammonium salt, etc. The cyclic chlorine derivatives of benzyl chloride include p-chlorobenzyl chloride and o-chlorobenzyl chloride and the like. P-chlorobenzyl chloride, also known as p-chlorobenzyl chloride, is an intermediate of medicine, pesticide insecticide, herbicide and dye, and can be used to pr...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C07C17/14C07C22/04
Inventor 乔旭崔咪芬汤吉海陈献
Owner NANJING UNIV OF TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products