Diethyl Ether → 2-Fluoro-1-phenylethan-1-one
Reaction equation
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:4].[F-:11].[K+].CCOCC>CN(C=O)C>[F:11][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:4]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
A mixture of 2-bromoacetophenone (20.00 gm, 100 mmol) and KF (8.82 gm, 152 mmol) in dry DMF (35 ml) was heated at 100° C. for 1 hour. Additional KF (2.26 gm) was added and heating of the mixture continued for 4 more hours. The dark-red solution was cooled, poured into Et2O and washed with H2O (twice) and brine. The ethereal solution was dried (Na2SO4), filtered, and stripped to yield a dark red oil. The oil was distilled to collect a fraction boiling between 62°-64° C. at 1 mm Hg which was 91 molar percent the title compound and 9 molar percent acetophenone (6.00 gm). Flash chromatography (Merck SiO2, 10% EtOAc in hexane) afforded the pure title compound (5.50 gm, 45%) as a liquid that solidifies near room temperature.
Workup
- temperatureheating of the mixture
- temperatureThe dark-red solution was cooled
- washwashed with H2O (twice) and brine
- dry with materialThe ethereal solution was dried (Na2SO4)
- filtrationfiltered
- customto yield a dark red oil
- distillationThe oil was distilled
- customto collect a fraction
- customboiling between 62°-64° C. at 1 mm Hg which
Sources & evidence
- ORD record
- ord-a0755630c49c44fb824718beceae1500
- Source dataset
- uspto-grants-1996_04
- Patent number
- US05506219
Reaction notes
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