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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466360Generated: October 29, 2026

Benzyl Alcohol → p-Toluenesulfonic acid

https://huagongshe.com/reaction/466360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantCalcium SulfateHCID 24497—
Reactant4-(4-Aminophenyl)butanoic acidHCID 27049—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventDiethyl EtherHCID 3283—
SolventCarbon TetrachlorideHCID 5943—
Productp-Toluenesulfonic acidHCID 6101—
Product4-(4-Aminophenyl)butyric acid benzyl esterHCID 54272448—

Reaction Steps

A mixture of 8.14 g (0.455 mol) of 4-(p-aminophenyl)butyric acid, 34.1 ml of benzyl alcohol and 8.65 g (0.455 mol) of p-toluene sulfonic acid hydrate in 115 ml of carbon tetrachloride is heated overnight at reflux with the solvent return through a tower of Drierite (ca. 30 ml of partially powdered indicating Drierite). The partially cooled mixture is diluted to 600 ml with ethyl ether to give a precipitate which is collected to give 4-(4-aminophenyl)butyric acid benzyl ester, p-toluenesulfonate; m.p. 114°-115° C. This is used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155268
Source datasetuspto-grants-1992_10
ORD IDord-e95fcabc17b447648e9214af064343fe
Source noteuspto-grants-1992_10