Diethyl Ether → 2-Fluoro-1-phenylethan-1-one

HRID 1720741Notes

Reaction equation

HRID 1720741 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

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

  1. temperatureheating of the mixture
  2. temperatureThe dark-red solution was cooled
  3. washwashed with H2O (twice) and brine
  4. dry with materialThe ethereal solution was dried (Na2SO4)
  5. filtrationfiltered
  6. customto yield a dark red oil
  7. distillationThe oil was distilled
  8. customto collect a fraction
  9. 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

Loading…