Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Preparation method of 2-methoxy-5-acetamidoaniline

A technology of acetamidoaniline and methoxy group, applied in the field of preparation of 2-methoxy-5-acetamidoaniline, can solve the problems of poor environmental protection, difficult catalyst or solvent recovery, low yield and the like

Inactive Publication Date: 2017-10-24
SHANGHAI ANOKY GRP +1
View PDF0 Cites 8 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] The technical problem to be solved in the present invention is to overcome the poor environmental protection, low yield, high cost, difficulty in catalyst or solvent recovery, long reaction time and high reaction temperature of the preparation method of 2-methoxy-5-acetamidoaniline in the prior art. high, poor safety, harsh reaction conditions and other defects, and a preparation method of 2-methoxy-5-acetamidoaniline is provided

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
  • Preparation method of 2-methoxy-5-acetamidoaniline
  • Preparation method of 2-methoxy-5-acetamidoaniline
  • Preparation method of 2-methoxy-5-acetamidoaniline

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0078] The preparation of embodiment 1 p-nitroanisole

[0079] Add 50 grams of sodium hydroxide and 60 grams of methanol to a 1000ml three-necked bottle, stir and heat up to 55°C, keep warm for 30 minutes to dissolve all the sodium hydroxide, then add 2 grams of tetrabutylammonium bromide, and control the temperature not to exceed 60°C Next, add 50 grams of p-chloronitrobenzene in batches, after the addition is complete, keep warm at 55-60°C for 1 hour, then raise the temperature to 60-70°C and keep warm for 4-5 hours, and control in HPLC until the raw material is less than 0.3%, which is the end of the reaction. Recover part of methanol (30 g under normal pressure), add 200 g of ice water under stirring, a large amount of yellow solid precipitates, filter, wash with water until neutral, and obtain 45 g of p-nitroanisole, yield 92.6%, GC purity 99.0%. The melting point is 53-54°C.

Embodiment 2

[0080] The preparation of embodiment 2 p-nitroanisole

[0081]In a 1000ml three-necked flask, add 40 grams of sodium hydroxide and 60 grams of methanol, stir and heat up to 55°C, keep warm for 30 minutes to dissolve all the sodium hydroxide, then add 2 grams of tetrabutylammonium bromide, and control the temperature not to exceed 60°C Next, add 50 grams of p-chloronitrobenzene in batches, after the addition is complete, keep warm at 55-60°C for 1 hour, then raise the temperature to 60-70°C and keep warm for 4-5 hours, and control in HPLC until the raw material is less than 0.3%, which is the end of the reaction. Recover part of methanol (30 g under normal pressure), add 200 g of ice water under stirring, a large amount of yellow solid precipitates, filter, wash with water until neutral, and obtain 45 g of p-nitroanisole, yield 91%, GC purity 98.9.0%. The melting point is 53-54°C.

[0082] Other experimental conditions and results are shown in the following table: Among them,...

Embodiment 3

[0084] The preparation of embodiment 3 p-nitroanisole

[0085] In a 1000mL three-necked flask, add 50g of sodium hydroxide and 30g of methanol recovered from Example 1 and 30g of new methanol and stir to raise the temperature to 55°C and keep it warm for 30 minutes to completely dissolve the sodium hydroxide, then add 2g of tetrabutylammonium bromide , under the condition that the temperature does not exceed 60°C, add 50 grams of p-chloronitrobenzene in batches, after the addition, keep it at 55-60°C for 1 hour, then raise the temperature to 60-70°C and keep it for 4-5 hours, and control the raw material in HPLC Less than 0.3% is the end point of the reaction. Recover 30 grams under normal pressure, add 200 grams of ice water under stirring, a large amount of yellow solid precipitates, filter, wash with water until neutral, and obtain 44.8 grams of p-nitroanisole, with a yield of 92.4% . Melting point 53-54°C, GC purity 99.1%.

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
melting pointaaaaaaaaaa
melting pointaaaaaaaaaa
melting pointaaaaaaaaaa
Login to View More

Abstract

The invention discloses a preparation method of 2-methoxy-5-acetamidoaniline. The preparation method comprises the following step: in a solvent, under the action of a catalyst Pd / C, performing a reduction reaction as shown below on a compound as shown in a formula 5 and hydrogen to obtain a compound as shown in a formula 6. The preparation method is low in pollution, high in yield rate, low in cost, convenient in catalyst or solvent recycling, short in reaction time, low in reaction temperature, high in safety and mild in reaction condition.

Description

technical field [0001] In particular, the present invention relates to a process for the preparation of 2-methoxy-5-acetamidoaniline. Background technique [0002] 2-Methoxy-5-acetamidoaniline is an important intermediate in the production of dyes and medicines. It can be used in the synthesis of various disperse dyes such as C.I. Disperse Blue 79 and C.I. Disperse Blue 301, and occupies an important position in the dye industry. [0003] The traditional process of synthesizing 2-methoxy-5-acetamidoaniline such as: [0004] 1. In [3-amino-4-methoxyacetanilide new synthesis process, Dyestuff Industry, 2001, 38(5): 28-29], 2,4-dinitrochlorobenzene was used as raw material and treated with methoxy 2,4-Dinitroanisole is obtained by hydrogenation, then catalytic hydrogenation, and finally acetylation; this synthesis route has two amino groups in the product after hydrogenation reduction, and it can be acetylated in one step in the acetylation reaction The sites are difficult to...

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): C07C233/43C07C231/12
CPCY02P20/584C07C231/12C07C233/43
Inventor 燕美芳赵敏尹东杨建王雪亮
Owner SHANGHAI ANOKY GRP
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com