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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276174Generated: November 1, 2026

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

https://huagongshe.com/reaction/1276174

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 numberUS06166011
Source datasetuspto-grants-2000_12
ORD IDord-5ba44b79ebc14144adbcae555f6eda15
Source noteuspto-grants-2000_12