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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975248Generated: November 1, 2026

Benzyl Alcohol → Benzyl 4-bromobutanoate

https://huagongshe.com/reaction/1975248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactant4-MethylmorpholineHCID 7972—
Reactant4-Bromobutyryl chlorideHCID 70225—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 4-bromobutanoateHCID 383248991%

Reaction Conditions

Temperature-20 °C

Reaction Steps

In the first step, 4-bromobutyryl chloride (13.8 g, 75 mmole) was placed in a 100 ml round bottom flask. The flask was cooled to -20° C. using a dry ice/carbon tetrachloride bath. Ethyl acetate (50 ml) containing N-methylmorpholine (7.58 g, 75 mmol, 8.2 ml) was added carefully. Using an addition funnel, benzyl alcohol (6.97 g, 6.67 ml, 6.64 mmoles) was added dropwise. After the addition the bath was removed and the mixture was stirred for 2 hours. The product was transferred to a separatory funnel using ethyl acetate (50 ml), washed once with sodium bicarbonate (10%), then twice with water, and dried with anhydrous sodium sulfate. Evaporation of solvents gave benzyl-4-bromo-butyrate as an oil (yield=91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05284951
Source datasetuspto-grants-1994_02
ORD IDord-0c49cec8733c47da8d9ce7debdfc4ed9
Source noteuspto-grants-1994_02