Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376164Generated: October 26, 2026

Acetyl chloride → Benzyl 4-acetoxypentanoate

https://huagongshe.com/reaction/376164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantBenzyl 4-hydroxypentanoateHCID 18991533—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-acetoxypentanoateHCID 18991525—

Reaction Conditions

Temperature0 °C

Reaction Steps

63 g (302.5 mmol) of benzyl 4-hydroxypentanoate and 46.4 ml (332.8 mmol) of triethylamine are charged under nitrogen at room temperature to 300 ml of CH2Cl2. The mixture is cooled to 0° C. and 21.5 ml (302.5 mmol) of acetyl chloride are added dropwise at 0°-5° C. When the dropwise addition is complete, the ice bath is removed and stirring is continued overnight at room temperature. The reaction mixture is mixed with ice-water and the organic phase is separated and washed twice with water. The aqueous phases are extracted twice with CH2Cl2. The organic phases are combined, dried over MgSO4, filtered and concentrated by evaporation. Distillation of the residue gives benzyl 4-acetoxypentanoate as a colourless oil of b.p. 126°-127° C./2.10-2 torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05488140
Source datasetuspto-grants-1996_01
ORD IDord-14187e328a334528a365a158b23a0e6f
Source noteuspto-grants-1996_01