5-Methoxy-2-fluorobenzyl cyanide

5-Methoxy-2-fluorobenzyl cyanide Suppliers list
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Tel: 021-54306202 13764082696
Email: info@hanhongsci.com
Company Name: Shandong Xiya Chemical Co., Ltd  
Tel: 13355009207 13355009207
Email: 3007715519@qq.com
Company Name: Shanghai Topbiochem Technology Co., Ltd  
Tel: +86-21-60341587
Email: sales@topbiochem.com
Company Name: SuZhou ShiYa Biopharmaceuticals, Inc.  
Tel: 86(512)5235 8471 17715136450
Email: sales@shiyabiopharm.com
Company Name: SynAsst Chemical.  
Tel: 021-60343070
Email:
5-Methoxy-2-fluorobenzyl cyanide Basic information
Product Name:5-Methoxy-2-fluorobenzyl cyanide
Synonyms:Benzeneacetonitrile, 2-fluoro-5-methoxy- (9CI);2-Fluoro-5-methoxybenzeneacetonitrile;2-(2-fluoro-5-Methoxyphenyl)acetonitrile;2-Fluoro-5-methoxyphenylacetonitrile97%;2-Fluoro-5-methoxybenzyl cyanide, (2-Fluoro-5-methoxyphenyl)acetonitrile;2-Fluoro-5-methoxyphenylacetonitrile 97%;Benzeneacetonitrile, 2-fluoro-5-methoxy-
CAS:672931-28-1
MF:C9H8FNO
MW:165.16
EINECS:
Product Categories:Fluorine series;METHOXY;HALIDE
Mol File:672931-28-1.mol
5-Methoxy-2-fluorobenzyl cyanide Structure
5-Methoxy-2-fluorobenzyl cyanide Chemical Properties
Boiling point 279℃
density 1.148
Fp 122℃
storage temp. Sealed in dry,Room Temperature
form crystalline powder
color White
Safety Information
HS Code 2909309090
MSDS Information
5-Methoxy-2-fluorobenzyl cyanide Usage And Synthesis
Synthesis
sodium:cyanide

773837-37-9

Benzene, 2-(broMoMethyl)-1-fluoro-4-Methoxy-

91319-42-5

5-Methoxy-2-fluorobenzyl cyanide

672931-28-1

General procedure for the synthesis of 2-fluoro-5-methoxyphenylacetonitrile from the compound (CAS: 773837-37-9) and 2-fluoro-5-methoxybenzyl bromide: Sodium cyanide (362 mg, 7.53 mmol) was added to a solution of compound 4 (1.5 g, 6.84 mmol) in anhydrous ethanol (15 mL), and the reaction mixture was stirred for 2 hr at 85 °C. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the complete consumption of the raw materials, the reaction mixture was concentrated to obtain the crude product. The crude product was diluted with ice water (30 mL) and extracted with ethyl acetate (2 x 50 mL). The organic layers were combined, washed with brine (20 mL), dried over anhydrous sodium sulfate and concentrated to give the residue. The residue was purified by rapid chromatography on silica gel (eluent: petroleum ether/ethyl acetate, gradient gradually increased from 100/0 to 70/30) to afford compound 5 (1 g, 90% yield) as a colorless liquid.1H NMR (400 MHz, DMSO-d6) δ: 7.21 (t, J = 9.2 Hz, 1H), 7.01 (dd, J = 6.1, 3.1 Hz, 1H), 6.94 (m, 1H), 4.01 (s, 2H), 3.75 (s, 3H). Mass spectrum (ESI) m/z: 166.06 [M+H]+.

References[1] Patent: WO2014/52365, 2014, A1. Location in patent: Page/Page column 302-303
5-Methoxy-2-fluorobenzyl cyanide Preparation Products And Raw materials
Raw materialssodium:cyanide-->Benzene, 2-(broMoMethyl)-1-fluoro-4-Methoxy-
Tag:5-Methoxy-2-fluorobenzyl cyanide(672931-28-1) Related Product Information
Benzeneacetonitrile 2,6-DIFLUORO-3-METHOXYPHENYLACETONITRILE 2-CHLORO-6-FLUORO-3-METHOXYPHENYLACETONITRILE (2-FLUORO-4,5-DIMETHOXYPHENYL)-(R)-HYDROXYACETONITRILE 2-FLUORO-5-(TRIFLUOROMETHOXY)PHENYLACETONITRILE 5-Methoxy-2-fluorobenzyl cyanide