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145908-29-8

145908-29-8 Structure

145908-29-8 Structure
IdentificationBack Directory
[Name]

2-BROMOMETHYL-4-CHLORO-BENZOIC ACID METHYL ESTER
[CAS]

145908-29-8
[Synonyms]

Methyl 2-(broMoMethyl)-4-chlorobenzoate
2-BROMOMETHYL-4-CHLORO-BENZOIC ACID METHYL ESTER
Benzoic acid, 2-(broMoMethyl)-4-chloro-, Methyl ester
[Molecular Formula]

C9H8BrClO2
[MDL Number]

MFCD11505950
[MOL File]

145908-29-8.mol
[Molecular Weight]

263.52
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H317-H319
[Precautionary statements ]

P280-P305+P351+P338
[RIDADR ]

3261
[HazardClass ]

8
[PackingGroup ]

Hazard InformationBack Directory
[Synthesis]

4-CHLORO-2-METHYL-BENZOIC ACID METHYL ESTER

99585-12-3

2-BROMOMETHYL-4-CHLORO-BENZOIC ACID METHYL ESTER

145908-29-8

Methyl 4-chloro-2-methylbenzoate (10.86 g, 58.8 mmol, 1.0 eq.) was used as the starting material and dissolved in carbon tetrachloride (100 mL). N-bromosuccinimide (15.7 g, 88.2 mmol, 1.5 eq.) and benzoyl peroxide (0.05 g) were added sequentially. The reaction mixture was heated to reflux overnight. After completion of the reaction, the reaction mixture was filtered and the solids were washed with dichloromethane. The organic filtrates were combined, concentrated and dried to afford the target product methyl 2-bromomethyl-4-chlorobenzoate (7.1 g, 45.8% yield). The structure of the product was confirmed by 1H NMR.

[References]

[1] Patent: US2005/143348, 2005, A1. Location in patent: Page/Page column 45; 49; 55
[2] Patent: US2005/239838, 2005, A1. Location in patent: Page/Page column 41
[3] Patent: WO2005/54176, 2005, A1. Location in patent: Page/Page column 136
[4] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 5, p. 1628 - 1631
[5] Patent: US2009/270393, 2009, A1. Location in patent: Page/Page column 43-44
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