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193290-19-6

193290-19-6 Structure

193290-19-6 Structure
IdentificationBack Directory
[Name]

methyl 2-(4-bromo-2-fluorophenyl)acetate
[CAS]

193290-19-6
[Synonyms]

Methyl 2-(4-bromo-2-fluorophenyl)
methyl 2-(4-bromo-2-fluorophenyl)acetate
Methyl 4-broMo-2-fluorophenylacetate, 96%
4-bromo-2-fluorophenylacetic acid methyl ester
Benzeneacetic acid, 4-bromo-2-fluoro-, methyl ester
[Molecular Formula]

C9H8BrFO2
[MDL Number]

MFCD20483545
[MOL File]

193290-19-6.mol
[Molecular Weight]

247.061
Chemical PropertiesBack Directory
[Boiling point ]

265.4±25.0 °C(Predicted)
[density ]

1.519±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

Solid
[Appearance]

Colorless to light yellow Liquid
[CAS DataBase Reference]

193290-19-6
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[HS Code ]

2918300090
Spectrum DetailBack Directory
[Spectrum Detail]

methyl 2-(4-bromo-2-fluorophenyl)acetate(193290-19-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

4-Bromo-2-fluorophenylacetic acid

114897-92-6

methyl 2-(4-bromo-2-fluorophenyl)acetate

193290-19-6

The general procedure for the synthesis of methyl 2-fluoro-4-bromophenylacetate from methanol and 2-fluoro-4-bromophenylacetic acid was as follows: a mixture of 2-fluoro-4-bromophenylacetic acid (20.2 g, 86.6 mmol) and concentrated sulfuric acid (7 mL) in methanol (200 mL) was heated and refluxed for 18 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in dichloromethane (200 mL), washed sequentially with saturated sodium bicarbonate solution and brine, and the organic phase was dried with anhydrous sodium sulfate. After filtration, the organic phase was concentrated under reduced pressure to give methyl 2-fluoro-4-bromophenylacetate (21.1 g, 99% yield) as a brown oil. Mass spectrum (ESI): m/z = 280.1 [M + H]+.

[References]

[1] Patent: WO2017/108723, 2017, A2. Location in patent: Page/Page column 225; 226
[2] Patent: US2014/194383, 2014, A1. Location in patent: Paragraph 0386-0388; 0390
[3] Patent: WO2014/141187, 2014, A1. Location in patent: Page/Page column 54; 55
[4] Patent: WO2016/38519, 2016, A1. Location in patent: Page/Page column 36; 37
[5] Patent: WO2016/38552, 2016, A1. Location in patent: Page/Page column 51
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