(3-BROMOPHENYL)ACETIC ACID METHYL ESTER
(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
(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
(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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