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

Novel method for preparing cinnoline derivative midbody dichloro dimethyl benzoquinone

A technology of dichlorodimethylbenzoquinone and dimethylbenzoquinone, which is applied in the field of new preparation of cinnoline derivative intermediates, can solve the problems of serious environmental pollution, low yield, waste acid water, etc., and achieve reaction The effect of high total yield, environmental friendliness and low production cost

Inactive Publication Date: 2014-05-14
湖南华腾制药有限公司
View PDF0 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The shortcoming of this method: 1, yield is lower, less than 20%
2. A lot of waste acid water is produced, causing serious environmental pollution

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
  • Novel method for preparing cinnoline derivative midbody dichloro dimethyl benzoquinone
  • Novel method for preparing cinnoline derivative midbody dichloro dimethyl benzoquinone
  • Novel method for preparing cinnoline derivative midbody dichloro dimethyl benzoquinone

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] (1) Preparation of dimethylbenzoquinone

[0021] Add 24.4g of 2,3-xylenol to 150ml of acetone, slowly add 60ml of 30% hydrogen peroxide dropwise, stir at room temperature for 24 hours, concentrate under reduced pressure to remove acetone, add ethyl acetate and water, carry out extraction and separation, collect the organic phase, and dry , concentrated, and the residue was recrystallized from ethyl acetate-petroleum ether (volume ratio 1:2) to obtain 22.6 g of compound 2 as a yellow solid (yield 83.08%).

[0022] (2) Preparation of Dichlorodimethylbenzoquinone

[0023] Dissolve 22g of dimethylbenzoquinone in 200ml of acetic acid, stir, heat to reflux, feed chlorine gas, react for 5 hours, stop the reaction, remove most of the acetic acid under reduced pressure, then add ethyl acetate and water for extraction and liquid separation, The organic phase was collected, dried, concentrated, and the residue was separated on a silica gel column to obtain 29 g of dichlorodimethy...

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

No PUM Login to View More

Abstract

The invention relates to a cinnoline derivative midbody, in particular to a novel method for preparing cinnoline derivative midbody dichloro dimethyl benzoquinone. 2, 3-xylenol is adopted as starting raw materials in the method, and target compounds are obtained through oxidization and chlorination.

Description

technical field [0001] The invention relates to a novel preparation method of a cinnoline derivative intermediate, in particular to a novel preparation method of dichlorodimethylbenzoquinone. technical background [0002] Dichlorodimethylbenzoquinone, chemical name 2,3-dichloro-5,6-dimethylcyclohexa-2,5-diene-1,4-dione, CAS: 15707-31-0, structural formula: [0003] [0004] Cinnoline derivatives are a class of compounds that play an important role in the pharmaceutical field, especially for bacterial and fungal fungicides. Dichlorodimethylbenzoquinone is an important intermediate in the synthesis of cinnoline derivatives. At present, the usual synthesis method is: add dimethylbenzoquinone to concentrated hydrochloric acid, heat and stir, then add concentrated nitric acid, continue heating and stirring for 2 hours, cool to room temperature, add ethyl acetate for extraction, collect the organic phase, dry, Concentrate to obtain a crude product, and then recrystallize to o...

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
IPC IPC(8): C07C46/00C07C50/24
CPCC07C46/00C07C46/06C07C50/24C07C50/02
Inventor 陈芳军邓泽平
Owner 湖南华腾制药有限公司
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