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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733694Generated: October 30, 2026

Phenylmethanesulfonyl chloride → HCID 20300035, compound

https://huagongshe.com/reaction/1733694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylmethanesulfonyl chlorideHCID 74740—
Reactant6-Chloro-1-hydroxy-1H-benzotriazoleHCID 232711—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventSodium HydroxideHCID 14798—
ProductHCID 20300035HCID 2030003556.5%

Reaction Steps

In 1 N aqueous sodium hydroxide (13.0 ml) and water is dissolved 1-hydroxy-6-chloro-1,2,3-benzotriazole (2.23 g) and thereto is added dropwise a solution of benzylsulfonyl chloride (2.5 g) in ether (50 ml) under ice-cooling and stirring, and the mixture is stirred at the same temperature for 1.5 hours and further at room temperature for 1 hour. The reaction mixture is distilled to remove ether. To the resulting residue is added ethyl acetate. The ethyl acetate layer is dried and distilled to remove the solvent. The residue is recrystallized from benzene-n-hexane to give white needles of 1-benzylsulfonyloxy-6-chloro-1,2,3-benzotriazole (2.4 g), melting point: 126.5°-127.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242507
Source datasetuspto-grants-1980_12
ORD IDord-2bbd2f5d491a477e895b20f26d3133e0
Source noteuspto-grants-1980_12