1-Bromo-2-ethyl-4-methoxy-benzene

1-Bromo-2-ethyl-4-methoxy-benzene Suppliers list
Company Name: Shanghai Jian Chao Chemical Technology Co., Ltd.  
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Email: 983544897@qq.com
Company Name: BePharm Ltd  
Tel: 400-685-9117
Email: market@bepharm.com
Company Name: Amadis Chemical Company Limited  
Tel: 571-89925085
Email: sales@amadischem.com
Company Name: Shanghai Pingguo Pharmaceutical Co., Ltd.  
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Company Name: Beijing YiboYuntian Technology Co., Ltd.  
Tel: 13811826434
Email: lichen13811826434@126.com

1-Bromo-2-ethyl-4-methoxy-benzene manufacturers

1-Bromo-2-ethyl-4-methoxy-benzene Basic information
Product Name:1-Bromo-2-ethyl-4-methoxy-benzene
Synonyms:Benzene, 1-bromo-2-ethyl-4-methoxy-;4-bromo-3-ethyl-1-methoxybezene;4-Bromo-3-ethylanisole;1-Bromo-2-ethyl-4-methoxy-benzene
CAS:34881-44-2
MF:C9H11BrO
MW:215.09
EINECS:
Product Categories:
Mol File:34881-44-2.mol
1-Bromo-2-ethyl-4-methoxy-benzene Structure
1-Bromo-2-ethyl-4-methoxy-benzene Chemical Properties
storage temp. Sealed in dry,Room Temperature
AppearanceColorless to light yellow Liquid
Safety Information
MSDS Information
1-Bromo-2-ethyl-4-methoxy-benzene Usage And Synthesis
Synthesis
3-Ethylphenyl(methyl) ether

10568-38-4

1-BROMO-2-ETHYL-4-METHOXY-BENZENE

34881-44-2

General procedure for the synthesis of 1-bromo-2-ethyl-4-methoxybenzene from 1-ethyl-3-methoxybenzene: 3-ethylanisole (50 g, 0.3676 mol) and N-bromosuccinimide (72 g, 0.4 mol) were dissolved in acetonitrile (1 L), and the reaction was stirred for 8 hours at room temperature protected from light. After completion of the reaction, the reaction mixture was concentrated at a temperature below 40 °C. The concentrated residue was redissolved in carbon tetrachloride and filtered to remove insoluble material. The filtrate was concentrated and finally the target product was obtained by fractional purification. A light yellow liquid product of 35 g was obtained in 43% yield.

References[1] Bulletin of the Chemical Society of Japan, 1989, vol. 62, # 2, p. 591 - 593
[2] Patent: US2006/4222, 2006, A1. Location in patent: Page/Page column 1; 3; 5
[3] Journal of Medicinal Chemistry, 2009, vol. 52, # 23, p. 7788 - 7799
1-Bromo-2-ethyl-4-methoxy-benzene Preparation Products And Raw materials
Raw materials3-Ethylphenyl(methyl) ether-->N-Bromosuccinimide-->Acetonitrile
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