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

HRID 1164814Notes

Reaction equation

HRID 1164814 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 ice-hydrochloric 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. stirringThe two phase mixture was vigorously stirred at room temperature for 11/2 hours
  4. customseparated
  5. washthe aqueous layer washed with dichloromethane (2×50 ml)
  6. washThe combined organic extracts were then washed with aqueous sodium hydroxide (3N, 2×100 ml), water (1×100 ml) and brine (1×100 ml)
  7. dry with materialdried (MgSO4)
  8. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-0939806affb9450aa3497160bfbb1fd7
Source dataset
uspto-grants-1990_03
Patent number
US04906628

Reaction notes

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