Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790752Generated: October 30, 2026

Benzyl Alcohol → Benzyl 4-bromobutanoate

https://huagongshe.com/reaction/1790752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
Reactant4-Bromobutyric acidHCID 75809—
ReactantSodium BicarbonateHCID 516892—
SolventThionyl ChlorideHCID 24386—
ProductBenzyl 4-bromobutanoateHCID 3832489—

Reaction Conditions

Temperature-50 °C

Reaction Steps

4-bromobutyric acid (10.6 g, 60 mmole) was dissolved in thionyl chloride (20 mml), and the reaction was kept for 4 hr. The solution was evaporated and coevaporated with toluene several times. The residue was redissolved in dichloromethane (120 ml), and then benzyl alcohol (4.14 ml, 40 mmole) was added. The solution was cooled down to −50° C. and triethylamine (10 ml, 72 mmole) was added. The reaction mixture was slowly warmed to room temperature. After 3 hr, the reaction mixture was poured into sodium bicarbonate aqueous solution and the organic phase was washed with water and dried, giving the titled product, 6.8 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071173B2
Source datasetuspto-grants-2006_07
ORD IDord-3d76282a1f9143b792bd2547fb2fed39
Source noteuspto-grants-2006_07