Basic information Safety Supplier Related

(3-BROMOPHENYL)ACETIC ACID METHYL ESTER

Basic information Safety Supplier Related

(3-BROMOPHENYL)ACETIC ACID METHYL ESTER Basic information

Product Name:
(3-BROMOPHENYL)ACETIC ACID METHYL ESTER
Synonyms:
  • (3-BROMOPHENYL)ACETIC ACID METHYL ESTER
  • Methyl 3-bromophenylacetate 98%
  • Methyl 3-bromophenylacetate
  • 3-Bromophenylacetic acid methyl ester, Methyl 2-(3-bromophenyl)ethanoate
  • Methyl3-bromophenylacetate98%
  • METHYL 2-(3-BROMOPHENYL)ACETATE
  • methyl 2-(3-bromophenyl)acetatee
  • Benzeneacetic acid, 3-bromo-, methyl ester
CAS:
150529-73-0
MF:
C9H9BrO2
MW:
229.07
Product Categories:
  • blocks
  • Bromides
  • Carboxes
  • pharmacetical
Mol File:
150529-73-0.mol
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(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
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Harmful/Irritant/Keep Cold
HS Code 
2916399090
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(3-BROMOPHENYL)ACETIC ACID METHYL ESTER Usage And Synthesis

Uses

Methyl 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

67-56-1

1878-67-7

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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