Ethanol → Ethyl 4-phenyl-2-chlorobenzoate

HRID 478352Notes

Reaction equation

HRID 478352 reaction equation
[C:1]1([C:7]2[CH:12]=[CH:11][C:10](OS(C(F)(F)F)(=O)=O)=[C:9]([Cl:21])[CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1(P(C2C=CC=CC=2)CCCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH2:51]([OH:53])[CH3:52].C(N(CC)CC)C.CN(C)[CH:63]=[O:64]>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.CCCCCC.O>[C:1]1([C:7]2[CH:12]=[CH:11][C:10]([C:63]([O:53][CH2:51][CH3:52])=[O:64])=[C:9]([Cl:21])[CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

9

Conditions

Temperature
85 °C

Procedure

To a solution of 4-phenyl-2-chloro-1-trifluoromethylsulfonyloxybenzene (35 g) in dimethylformamide (300 ml) are added palladium acetate (1.17 g), 1,3-bis(diphenylphosphino)propane (4.29 g), ethanol (91.5 ml) and triethylamine (29.0 ml) under carbon monooxide atmosphere, and the mixture is heated with stirring at 80-90° C. for 6 hours. To the reaction solution is added water, and further added a small amount of n-hexane. The mixture is extracted with ethyl acetate, and the ethyl acetate layer is washed with water, dried, and the residue is purified by silica gel column chromatography (solvent; n-hexane→ethyl acetate:n-hexane=1:100) to give ethyl 4-phenyl-2-chlorobenzoate (20.9 g) as colorless oil.

Workup

  1. temperaturethe mixture is heated
  2. extractionThe mixture is extracted with ethyl acetate
  3. washthe ethyl acetate layer is washed with water
  4. customdried
  5. customthe residue is purified by silica gel column chromatography (solvent; n-hexane→ethyl acetate:n-hexane=1:100)

Sources & evidence

ORD record
ord-ec51087fe86f42ebbe691e01e523504a
Source dataset
uspto-grants-2003_11
Patent number
US06642223B2

Reaction notes

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