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788081-99-2

788081-99-2 Structure

788081-99-2 Structure
IdentificationBack Directory
[Name]

2-BROMOMETHYL-5-METHOXY-BENZOIC ACID METHYL ESTER
[CAS]

788081-99-2
[Synonyms]

Methyl 2-(broMoMethyl)-5-Methoxybenzoate
2-BROMOMETHYL-5-METHOXY-BENZOIC ACID METHYL ESTER
Benzoic acid, 2-(bromomethyl)-5-methoxy-, methyl ester
[Molecular Formula]

C10H11BrO3
[MDL Number]

MFCD11505947
[MOL File]

788081-99-2.mol
[Molecular Weight]

259.1
Chemical PropertiesBack Directory
[Boiling point ]

342.5±32.0 °C(Predicted)
[density ]

1.432±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
Hazard InformationBack Directory
[Synthesis]

5-METHOXY-2-METHYL-BENZOIC ACID METHYL ESTER

73502-03-1

2-BROMOMETHYL-5-METHOXY-BENZOIC ACID METHYL ESTER

788081-99-2

General procedure for the synthesis of methyl 2-bromomethyl-5-methoxybenzoate from methyl 2-methyl-5-methoxybenzoate: Preparation of intermediate 12: Compound 11 (4.4 g, 24.2 mmol) was dissolved in carbon tetrachloride (80 mL) and N-bromosuccinimide (4.48 g, 24.2 mmol) and benzoyl peroxide (276 mg 1.13 mmol). The reaction mixture was heated to reflux and stirred for 3 hours. After completion of the reaction, the solid insoluble material was removed by filtration and the filter cake was washed with ether. The organic phases were combined, washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the target product 12 (6.1 g, 98% yield). Product characterization data: mass spectrum (LCMS) m/z 260 ([M+H]+), 1H NMR (CDCl3) δ 4.50 (2H, s, CH2Br), 3.73 (3H, s, OCH3), 3.88 (3H, s, CO2CH3), 6.86-7.50 (m, 3H, Ar-H).

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 17, p. 5286 - 5289
[2] Patent: WO2009/14637, 2009, A2. Location in patent: Page/Page column 70
[3] Patent: WO2010/54279, 2010, A1. Location in patent: Page/Page column 100
[4] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 24, p. 7283 - 7287
[5] Patent: WO2006/138549, 2006, A1. Location in patent: Page/Page column 73
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