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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938103Generated: October 26, 2026

Acetic Acid → 1-Phenyl-3-acetoxybutane

https://huagongshe.com/reaction/1938103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
Reactant4-Phenyl-2-butanolHCID 61302—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
Product1-Phenyl-3-acetoxybutaneHCID 6151798.5%

Reaction Steps

Into a four-necked flask provided with a thermometer and a stirrer, 150 g (1 mol) of 4-phenyl-2-butanol (XXX-35), 500 ml of toluene and 200 ml of pyridine were charged. 122.4 g (1.2 mol) of anhydrous acetic acid and 1 g of 4-dimethylaminopyridine were further added thereto to react them 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 solution, extracted and fractionated, and then an organic layer was washed with 1N hydrochloric acid, water, 5% sodium bicarbonate solution and water in the order. The thus-obtained organic layer was concentrated under a reduced pressure to obtain 189 g of 2-acetoxy-4-phenylbutane (XXIX-35) with yield of 98.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05693251
Source datasetuspto-grants-1997_12
ORD IDord-c8c37081e6e1451cb431d8c9170b5a46
Source noteuspto-grants-1997_12