Ethyl 2-(2-bromophenyl)acetate

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Ethyl 2-(2-bromophenyl)acetate Basic information
Uses
Product Name:Ethyl 2-(2-bromophenyl)acetate
Synonyms:Benzeneacetic acid, 2-broMo-, ethyl ester;2-Bromophenylacetic acid ethyl ester;Ethyl 2-(2-bromophenyl)ethanoate;(2-Brom-phenyl)-essigsaeure-aethylester;Ethyl 2-bromobenzeneacetate;Ivankasse impurity 25;Ethyl (2-bromophenyl)acetate - [E72192]
CAS:2178-24-7
MF:C10H11BrO2
MW:243.1
EINECS:
Product Categories:
Mol File:2178-24-7.mol
Ethyl 2-(2-bromophenyl)acetate Structure
Ethyl 2-(2-bromophenyl)acetate Chemical Properties
Melting point 35-38℃
Boiling point 114 °C(Press: 4 Torr)
density 1.389±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
AppearanceColorless to off-white <35°C Solid,>36°C Liquid
Safety Information
RIDADR UN3261
HazardClass 8
PackingGroup II
HS Code 2915390090
MSDS Information
Ethyl 2-(2-bromophenyl)acetate Usage And Synthesis
UsesETHYL 2-(2-BROMOPHENYL)ACETATE is a useful research chemical.
Synthesis
Ethanol

64-17-5

2-Bromophenylacetic acid

18698-97-0

Ethyl 2-(2-bromophenyl)acetate

2178-24-7

GENERAL METHOD: 3 g (13.8 mmol) of o-bromophenylacetic acid was dissolved in 10 mL of ethanol and the solution was cooled to 0°C. The solution was then cooled to 0°C and the solution was then dried. Under stirring, 1.6 mL (22 mmol) of thionyl chloride was slowly added dropwise. After the dropwise addition was completed, the reaction mixture was gradually heated to 50 °C and kept at this temperature for the reaction overnight. Upon completion of the reaction, the mixture was cooled to room temperature and the solvent was subsequently evaporated under reduced pressure. The residue was mixed with ethyl acetate and filtered through a 6 g column of basic alumina. Finally, the filtrate was evaporated under reduced pressure to give 3.5 g (89% yield) of ethyl (2-bromophenyl) acetate (1d).

References[1] European Journal of Inorganic Chemistry, 2015, vol. 2015, # 10, p. 1752 - 1758
[2] Patent: WO2009/121919, 2009, A1. Location in patent: Page/Page column 163
[3] Synthesis (Germany), 2015, vol. 47, # 13, p. 1913 - 1921
[4] Organic Letters, 2005, vol. 7, # 22, p. 4963 - 4966
[5] Patent: WO2004/63150, 2004, A2. Location in patent: Page 28
Ethyl 2-(2-bromophenyl)acetate Preparation Products And Raw materials
Raw materials1-Bromo-2-iodobenzene-->Ethanol-->2-Bromophenylacetic acid-->EthoxycarbonylMethylzinc broMide
Preparation ProductsEthyl 10-methyl-9-phenanthrenecarboxylate
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