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111982-45-7

111982-45-7 Structure

111982-45-7 Structure
IdentificationBack Directory
[Name]

2-FLUOROPHENYL CYCLOPENTYL KETONE
[CAS]

111982-45-7
[Synonyms]

2-FLUOROPHENYL CYCLOPENTYL KETONE
Cyclopentyl-(2-Fluorophenyl)methanone
Methanone, cyclopentyl(2-fluorophenyl)-
[Molecular Formula]

C12H13FO
[MDL Number]

MFCD03841320
[MOL File]

111982-45-7.mol
[Molecular Weight]

192.23
Chemical PropertiesBack Directory
[Boiling point ]

275.8±13.0 °C(Predicted)
[density ]

1.131±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Oil
[color ]

Colourless
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

2-Fluorophenyl cyclopentyl ketone is a precursor in the synthesis of fluoroketamine.
[Synthesis]

2-Fluorobenzonitrile

394-47-8

CYCLOPENTYLMAGNESIUM BROMIDE

33240-34-5

2-FLUOROPHENYL CYCLOPENTYL KETONE

111982-45-7

General procedure for the synthesis of 2-fluorophenylcyclopentanone from 2-fluorobenzonitrile and cyclopentylmagnesium bromide: 2-fluorobenzonitrile (5.0 g, 41.01 mmol) was added to 80 mL of THF containing 2 moles of cyclopentylmagnesium bromide in THF solution (20.51 mL, 41.01 mmol) and CuBr (0.100 g) under argon protection at 60 °C and the reaction was The reaction was stirred for 15 hours. After completion of the reaction, the reaction mixture was cooled to 0 °C, 5% sulfuric acid solution was added, and stirring was continued for 15 hours. Subsequently, the reaction mixture was extracted with ether three times. The organic layers were combined, dried with anhydrous MgSO4, concentrated and the residue was purified by column chromatography (eluent: a mixture of ethyl acetate and hexane) to afford the target product 2-fluorophenyl cyclopentanone (3.085 g, 40% yield). The mass spectrum (ES) showed m/z=192.15 (M+1)+.

[References]

[1] Patent: WO2005/66126, 2005, A1. Location in patent: Page/Page column 83
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