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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298857Generated: November 2, 2026

Thionyl Chloride → 2-Chloro-1,3-benzoxazol-6-OL

https://huagongshe.com/reaction/2298857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 178515778HCID 178515778—
SolventDimethylformamideHCID 6228—
Product2-Chloro-1,3-benzoxazol-6-OLHCID 23441246—

Reaction Steps

2-Sulfanyl-1,3-benzoxazol-6-ol (2.08 g) [see Preparation 33] was added to thionyl chloride (12.3 ml), followed by dimethylformamide (0.93 ml). The reaction mixture was heated to reflux for 5 minutes, after which time the mixture was allowed to cool. The solvent was removed under reduced pressure, the residue azeotroped twice with xylene, and the residue then partitioned between diethyl ether and water. The organic layer was separated, dried over magnesium sulphate and the solvent removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 100:0 changing to 0:100, by volume, hexane: ethyl acetate in 50% increments to afford 2-chloro-1,3-benzoxazol-6-ol (1.715 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495549B1
Source datasetuspto-grants-2002_12
ORD IDord-2d4bc7d8cc5e44c191e9ea425ba9cac8
Source noteuspto-grants-2002_12