Fluorobenzene → 2-Chloro-1-(4-fluorophenyl)propan-1-one

HRID 5809

Reaction equation

HRID 5809 reaction equation
[Cl:1][CH:2]([CH3:6])[C:3](Cl)=[O:4].[Cl-].[Cl-].[Cl-].[Al+3].[F:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>ClCCl>[Cl:1][CH:2]([CH3:6])[C:3]([C:15]1[CH:16]=[CH:17][C:12]([F:11])=[CH:13][CH:14]=1)=[O:4]

Participants

5

Procedure

A solution of 2-chloropropionyl chloride (49 ml) in dichloromethane (50 ml) was added to a mixture of anhydrous aluminium trichloride (55.5 g) in dichloromethane (120 ml). The mixture was stirred for 10 minutes at room temperature and then a solution of fluorobenzene (39.5 ml) in dichloromethane (30 ml) was added dropwise. The resulting mixture was stirred for one hour, allowed to stand for 16 hours and then poured on to an icehydrochloric acid mixture. The two phase mixture was vigorously stirred at room temperature for 11/2 hours, separated and the aqueous layer washed with dichloromethane (2×50 ml). The combined organic extracts were then washed with aqueous sodium hydroxide (3N, 2×100 ml), water (1×100 ml) and brine (1×100 ml), dried (MgSO4) and evaporated under reduced pressure to afford 2-chloro-1-(4-fluorophenyl)-1-propanone, 71.3 g.

Workup

  1. stirringThe resulting mixture was stirred for one hour
  2. waitto stand for 16 hours
  3. additionpoured on to an icehydrochloric acid mixture
  4. stirringThe two phase mixture was vigorously stirred at room temperature for 11/2 hours
  5. customseparated
  6. washthe aqueous layer washed with dichloromethane (2×50 ml)
  7. washThe combined organic extracts were then washed with aqueous sodium hydroxide (3N, 2×100 ml), water (1×100 ml) and brine (1×100 ml)
  8. dry with materialdried (MgSO4)
  9. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-6a06c5f7ca494a2a99419033715c3d96
Source dataset
uspto-grants-1993_09
Patent number
US05246928

Linked notes

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