2-Chlorophenol → 2-Chlorophenyl propionate

HRID 1362517Notes

Reaction equation

HRID 1362517 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].C(N(CC)CC)C.[C:16](Cl)(=[O:19])[CH2:17][CH3:18]>ClCCl>[C:16]([O:8][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[Cl:1])(=[O:19])[CH2:17][CH3:18]

Participants

5

Procedure

A solution, cooled to 10° C., of 2-chlorophenol (100 g, 0.778 mol) in 250 ml of dichloromethane is slowly admixed with triethylamine (120.7 ml). A solution of 60.7 ml of propionyl chloride in 60 ml of dichloromethane is added slowly dropwise to this mixture over the course of an hour. Following the addition of the propionyl chloride, the mixture is allowed to come slowly to room temperature and is stirred at room temperature for a total of five hours. Following removal of the triethylammonium chloride by filtration, the filtrate is diluted with 100 ml of dichloromethane and washed with 0.1 N hydrochloric acid (500 ml), 0.1 M aqueous sodium hydroxide solution (500 ml) and water (500 ml). The organic phase is dried over sodium sulphate (100 g) for three hours. After the drying agent has been removed by filtration, the solvent is removed on a rotary evaporator. Distillation of the oily yellow residue under reduced pressure gives 129.2 g (90% yield) of 2-chlorophenyl propionate as a colourless liquid (bp 90-93° C./0.3 mm).

Workup

  1. customto come slowly to room temperature
  2. customremoval of the triethylammonium chloride
  3. filtrationby filtration
  4. additionthe filtrate is diluted with 100 ml of dichloromethane
  5. washwashed with 0.1 N hydrochloric acid (500 ml), 0.1 M aqueous sodium hydroxide solution (500 ml) and water (500 ml)
  6. dry with materialThe organic phase is dried over sodium sulphate (100 g) for three hours
  7. customAfter the drying agent has been removed by filtration
  8. customthe solvent is removed on a rotary evaporator
  9. distillationDistillation of the oily yellow residue under reduced pressure

Sources & evidence

ORD record
ord-7c371b4df8314d57af765d09e56bf10c
Source dataset
uspto-grants-2011_02
Patent number
US07880042B2

Reaction notes

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