4-Toluenesulfonyl chloride → Toluene-4-sulfonic acid (S)-2-phenyl-propyl ester

HRID 1260202Notes

Reaction equation

HRID 1260202 reaction equation
[C:1]1([C@H:7]([CH3:10])[CH2:8][OH:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:11]1([CH3:21])[CH:16]=[CH:15][C:14]([S:17](Cl)(=[O:19])=[O:18])=[CH:13][CH:12]=1>ClCCl>[C:1]1([C@H:7]([CH3:10])[CH2:8][O:9][S:17]([C:14]2[CH:15]=[CH:16][C:11]([CH3:21])=[CH:12][CH:13]=2)(=[O:19])=[O:18])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

4

Reactant 2

HCID 73974-Toluenesulfonyl chlorideHCID 4476612-Phenylpropanol

Product 1

HCID 13791931Toluene-4-sulfonic acid (S)-2-phenyl-propyl esterYield 100.9%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 20 g of (S)-(−)-2-phenyl-1-propanol in 240 ml of dichloromethane was added in portions 28 g of p-toluenesulfonyl chloride (146.8 mmol). After stirring for 18 h at room temperature, the organic phase was washed with 100 ml of water, dried over magnesium sulfate, filtered, and the solvent evaporated under reduced pressure to yield 43 g of the title compound.

Workup

  1. washthe organic phase was washed with 100 ml of water
  2. dry with materialdried over magnesium sulfate
  3. filtrationfiltered
  4. customthe solvent evaporated under reduced pressure

Sources & evidence

ORD record
ord-15069b6edfa34ff280a9d7d5e60ded58
Source dataset
uspto-grants-2013_06
Patent number
US08470810B2

Reaction notes

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