ChemicalBook--->CAS DataBase List--->1402412-84-3

1402412-84-3

1402412-84-3 Structure

1402412-84-3 Structure
IdentificationBack Directory
[Name]

2-Fluoro-1-(2-fluoro-phenyl)-ethanone
[CAS]

1402412-84-3
[Synonyms]

2-Fluoro-1-(2-fluoro-phenyl)-ethanone
Ethanone, 2-fluoro-1-(2-fluorophenyl)-
2-fluoro-1-(2-fluorophenyl)ethan-1-one
2-FLUORO-1-(2-FLUORO-PHENYL)-ETHANONE(WXFC0849)
[Molecular Formula]

C8H6F2O
[MDL Number]

MFCD24713349
[MOL File]

1402412-84-3.mol
[Molecular Weight]

156.13
Chemical PropertiesBack Directory
[storage temp. ]

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

2914790090
Hazard InformationBack Directory
[Synthesis]

Ethanone,1-(2-fluorophenyl)-2-hydroxy-(9CI)

218771-68-7

2-Fluoro-1-(2-fluoro-phenyl)-ethanone

1402412-84-3

The general procedure for the synthesis of 2-fluoro-1-(2-fluorophenyl)ethanone from 1-(2-fluorophenyl)-2-hydroxyacetophenone was as follows: 1-(2-fluorophenyl)-2-hydroxyacetophenone [CAS 218771-68-7] (2.77 g, 18.0 mmol) was dissolved in dichloromethane (42 ml), and triethylamine (6.36 g, 62.8 mmol), triethylamine trihydrofluoride (3.05 g, 18.0 mmol) and n-butyl ninafluoroacetylsulfonyl fluoride (8.48 g, 26.9 mmol) were added sequentially at 0 °C. The reaction tube was sealed and the reaction mixture was stirred at room temperature overnight. After completion of the reaction, the dark red solution was poured into a mixture of saturated sodium bicarbonate solution and ice and extracted with dichloromethane. The organic layer was separated, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by rapid chromatography on silica gel (Telos Flash Silica) using dichloromethane as eluent to afford 2-fluoro-1-(2-fluorophenyl)ethanone (1.23 g, 61% yield) as a yellow semi-solid.

[References]

[1] Patent: US2012/258962, 2012, A1. Location in patent: Page/Page column 29
[2] Patent: WO2012/139993, 2012, A1. Location in patent: Page/Page column 52
[3] Patent: WO2012/168164, 2012, A1. Location in patent: Page/Page column 36
[4] Journal of Medicinal Chemistry, 2013, vol. 56, # 10, p. 3980 - 3995
[5] Patent: WO2016/75064, 2016, A1. Location in patent: Page/Page column 24
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