Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728450Generated: November 2, 2026

Benzyl Alcohol → HCID 19018237, compound

https://huagongshe.com/reaction/1728450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant4-(Chloromethyl)benzoyl chlorideHCID 70136—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 19018237HCID 19018237—

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred suspension of 3.0 g (14 mmol) of 4-(bromomethyl)benzoic acid and 3.5 ml (41 mmol) of oxalyl chloride in 35 ml of dichloromethane was refluxed for 10 hours and cooled to room temperature. Evaporation afforded 4-(chloromethyl)benzoyl chloride as an oil which was used without purification. To a cooled (0° C.) solution of 2.6 g (14 mmol) of 4-(chloromethyl)benzoyl chloride and 2.0 g (18 mmol) of benzyl alcohol in 30 ml of dichloromethane was added 1.8 g (18 mmol) of triethylamine. The reaction was stirred at 0° C. for 0.2 hours, then at room temperature for an additional 1 hour and poured into 150 ml of EtOAc. The EtOAc layer was with three portions of water, dried over Na2SO4, filtered and evaporated. The crude product was flash chromatographed (5% EtOAc/hexanes) to give 0.7 g of product; m.p. 52°-54° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05326905
Source datasetuspto-grants-1994_07
ORD IDord-1128eb7441804bfdb2bf67f66940e54b
Source noteuspto-grants-1994_07