(3-Bromophenyl)acetic acid methyl ester

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(3-Bromophenyl)acetic acid methyl ester Basic information
Product Name:(3-Bromophenyl)acetic acid methyl ester
Synonyms:Methyl 3-bromophenylacetate 98%;3-Bromophenylacetic acid methyl ester, Methyl 2-(3-bromophenyl)ethanoate;Methyl3-bromophenylacetate98%;methyl 2-(3-bromophenyl)acetatee;Benzeneacetic acid, 3-bromo-, methyl ester;Methyl 2-(3-bromophenyl)acetate, 97%;METHYL 2-(3-BROMOPHENYL)ACETATE;Methyl 3-bromophenylacetate
CAS:150529-73-0
MF:C9H9BrO2
MW:229.07
EINECS:
Product Categories:blocks;Bromides;Carboxes;pharmacetical
Mol File:150529-73-0.mol
(3-Bromophenyl)acetic acid methyl ester Structure
(3-Bromophenyl)acetic acid methyl ester Chemical Properties
Boiling point 268.6±15.0 °C(Predicted)
density 1.445±0.06 g/cm3(Predicted)
refractive index 1.5440 to 1.5480
storage temp. Sealed in dry,Room Temperature
form clear liquid
color Colorless to Almost colorless
Safety Information
Hazard Codes Xi
Hazard Note Harmful/Irritant/Keep Cold
HS Code 2916399090
MSDS Information
(3-Bromophenyl)acetic acid methyl ester Usage And Synthesis
UsesMethyl 2-(3-bromophenyl)acetate is used as a reagent to synthesize the methyl ester derivative of (R)-Flurbiprofen (F598730). (R)-Flurbiprofen is a nonsteroidal anti-inflammatory drug that exists as a racemate and also has potential application as a treatment for patients with Alzheimer’s Disease.
Synthesis
Methanol

67-56-1

3-Bromophenylacetic acid

1878-67-7

(3-BROMOPHENYL)ACETIC ACID METHYL ESTER

150529-73-0

General procedure for the synthesis of methyl (3-bromophenyl)acetate from methanol and 3-bromophenylacetic acid: acetyl chloride (0.08 mL, 1.2 mmol, 0.5 eq.) and 3-bromophenylacetic acid (0.5 g, 2.3 mmol, 1.0 eq.) were added to methanol (10 mL), and the reaction mixture was refluxed for 2 hours. Upon completion of the reaction, the consumption of starting material was confirmed by TLC monitoring. The reaction mixture was concentrated and extracted with dichloromethane (DCM). The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford methyl (3-bromophenyl)acetate as a colorless oil (0.525 g, 98.7% yield). The product was analyzed by LC-MS (ES), m/z = 229.0, 231.0 [M + H]+. 1H NMR (400 MHz, DMSO-d6) δ 3.61 (s, 3H), 3.70 (s, 2H), 7.26-7.30 (m, 2H), 7.43-7.46 (m, 1H), 7.48 (s, 1H).

References[1] Bioorganic and Medicinal Chemistry, 2003, vol. 11, # 13, p. 2843 - 2866
[2] Journal of Medicinal Chemistry, 2008, vol. 51, # 3, p. 392 - 395
[3] Patent: EP1479681, 2004, A1. Location in patent: Page 111; 112
[4] Patent: US2007/3539, 2007, A1. Location in patent: Page/Page column 96
[5] Journal of Medicinal Chemistry, 1995, vol. 38, # 26, p. 4976 - 4984
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