(5-Chloro-2-methoxyphenyl)acetonitrile

(5-Chloro-2-methoxyphenyl)acetonitrile Suppliers list
Company Name: Shanghai Renshi Pharmatech Co., LTD  Gold
Tel: 021-61150625 18521367657
Email: info@renshipharma.com
Company Name: Nanjing Chemlin Chemical Co., Ltd  
Tel: 025-83697070 13770331960
Email: info@chemlin.com.cn
Company Name: SynAsst Chemical.  
Tel: 021-60343070
Email:
Company Name: ShangHai AmK Pharmaceutical Technology Co., Ltd.  
Tel: 微信 18019252918 18019252918
Email: sale@amkchem.com
Company Name: Changzhou Tianrui Pharmaceutical Technology Co., Ltd.  
Tel: 0519-85386832 13382812559
Email: sales@cztrchem.com
(5-Chloro-2-methoxyphenyl)acetonitrile Basic information
Product Name:(5-Chloro-2-methoxyphenyl)acetonitrile
Synonyms:2-(5-chloro-2-Methoxyphenyl)acetonitrile;Benzeneacetonitrile, 5-chloro-2-methoxy-;5-Chloro-2-methoxybenzeneacetonitrile
CAS:7048-38-6
MF:C9H8ClNO
MW:181.62
EINECS:
Product Categories:
Mol File:7048-38-6.mol
(5-Chloro-2-methoxyphenyl)acetonitrile Structure
(5-Chloro-2-methoxyphenyl)acetonitrile Chemical Properties
Melting point 63 °C(Solv: water (7732-18-5); ethanol (64-17-5))
Boiling point 138-140 °C(Press: 1 Torr)
density 1.198±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
AppearanceWhite to off-white Solid
Safety Information
HS Code 2926907090
MSDS Information
(5-Chloro-2-methoxyphenyl)acetonitrile Usage And Synthesis
Synthesis
sodium:cyanide

773837-37-9

4-CHLORO-2-(CHLOROMETHYL)-1-METHOXYBENZENE

7035-11-2

(5-CHLORO-2-METHOXYPHENYL)ACETONITRILE

7048-38-6

The general procedure for the synthesis of 5-chloro-2-methoxyphenylacetonitrile from the compound (CAS: 773837-37-9) and 4-chloro-2-(chloromethyl)-1-methoxybenzene was as follows: compound Z-0-6 (32 g, 168 mmol) was dissolved in dimethyl sulfoxide (DMSO, 200 mL). Subsequently, sodium cyanide (29 g, 606 mmol) was added to the solution. The reaction mixture was heated to 80 °C under nitrogen protection and maintained at this temperature for 3 hours. Upon completion of the reaction, the mixture was cooled to room temperature, dispersed by the addition of water, and the product was subsequently separated by diafiltration. The filter cake was washed with a small amount of water and dried to give Z-0-7 (31 g, yield: 98.3%) as an orange-red solid.

References[1] Patent: CN106243003, 2016, A. Location in patent: Paragraph 0130; 0131; 0136
[2] Patent: US2016/130239, 2016, A1. Location in patent: Paragraph 0735; 0739
[3] Patent: WO2014/151472, 2014, A1. Location in patent: Paragraph 00398-00399
[4] Patent: WO2016/40315, 2016, A1. Location in patent: Paragraph 00441; 00442
[5] Journal of Medicinal Chemistry, 2017, vol. 60, # 16, p. 7029 - 7042
(5-Chloro-2-methoxyphenyl)acetonitrile Preparation Products And Raw materials
Raw materialssodium:cyanide-->4-Chloro-2-(chloromethyl)-1-methoxybenzene
Tag:(5-Chloro-2-methoxyphenyl)acetonitrile(7048-38-6) Related Product Information
Benzeneacetonitrile ACETONE-D6 2-Methoxyphenylacetonitrile