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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240587Generated: November 2, 2026

4-Toluenesulfonyl chloride → 3-(4-Methylphenyl)propyl 4-methylbenzene-1-sulfonate

https://huagongshe.com/reaction/2240587

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-(4-Methylphenyl)propan-1-olHCID 221893—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product3-(4-Methylphenyl)propyl 4-methylbenzene-1-sulfonateHCID 5390330170%

Reaction Steps

2.46 g of tosyl chloride (13 mM), 3.4 ml of diisopropylamine (19.4 mM) and 158 mg of 4-(dimethylamino)pyridine (1.29 mM) were added to reaction solution (6.46 mM) dissolving 971 mg of 3-p-tolyl-propane-1-ol (40ac) prepared by above step 3 in methylene chloride at 0° C. under Ar atmosphere with stirring for 6 hrs, and the reaction mixture was stirred for 12 hrs at room temperature. After the reaction mixture was neutralized with ammonium chloride, the mixture was extracted with ethyl acetate, washed with saturated NaCl solution, dried over MgSO4, filtered, and concentrated in vacuo. The resultant was purified by Silica gel column chromatography with a solvent mixture mixed with methanol and chloroform (1:7) as an eluant to give 1.3 g of toluene-4-sulfonate-3-p-tolyl-propyl ester (40ad) (yield: 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723376B2
Source datasetuspto-grants-2010_05
ORD IDord-4c866b7f470947938e6e6aeda29eeaa8
Source noteuspto-grants-2010_05