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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274175Generated: October 27, 2026

Hydrochloric Acid → 3-Phenylbutyl acetate

https://huagongshe.com/reaction/274175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantAcetic AnhydrideHCID 7918—
ReactantBenzenepropanol, gamma-methyl-HCID 94243—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
Product3-Phenylbutyl acetateHCID 301645599%

Reaction Steps

Into a four-necked flask provided with a stirring means and a thermometer, 150 g (1 mol) of (+)-3-phenyl-l-butanol (XXVI-60), 500 ml of toluene and 200 ml of pyridine were charged, and 122.4 g (1.2 mol) of acetic acid anhydride and 1 g of 4-dimethylaminopyridine were further added thereto. The mixture was reacted for 4 hours while temperature being maintained at 40°-50° C. After completion of the reaction, the reaction mixture was poured into 500 ml of 4N hydrochloric acid, extracted and fractionated. The resulting organic layer was washed with 1N hydrochloric acid, water, 5% sodium bicarbonate aqueous solution ad water in the order. The thus-obtained organic layer was concentrated under a reduced pressure to obtain 190 g of (+)-1-acetoxy-3-phenylbutane (XXV-60) with yield of 99.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389293
Source datasetuspto-grants-1995_02
ORD IDord-f76910b5ff3a4b55841ed7ed7ae294c0
Source noteuspto-grants-1995_02