Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276175Generated: October 31, 2026

Acetic Anhydride → 2-Chloro-1,3-benzoxazol-6-yl acetate

https://huagongshe.com/reaction/1276175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-1,3-benzoxazol-6-OLHCID 23441246—
SolventDichloromethaneHCID 6344—
Product2-Chloro-1,3-benzoxazol-6-yl acetateHCID 18340179—

Reaction Steps

Triethylamine (1.48 ml) was added to a suspension of 2-chloro-1,3-benzoxazol-6-ol (1.63 g) [see Preparation 34] in dichloromethane (20 ml), and after 5 minutes acetic anhydride (1.01 ml) was added. The reaction mixture was stirred at room temperature for 18 hours, after which time the solvent was removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 100:0, changing 40:10, changing to 0:100, by volume, hexane:ethyl acetate to afford 2-chloro-1,3-benzoxazol-6-yl acetate (1.63 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166011
Source datasetuspto-grants-2000_12
ORD IDord-f05afbec90454e15a93f789a6f12d44d
Source noteuspto-grants-2000_12