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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21668Generated: October 29, 2026

Benzenesulfonyl chloride → N'-t-butyl-N-benzenesulfonyl-N'-benzoylhydrazine

https://huagongshe.com/reaction/21668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantN-(tert-butyl)benzohydrazideHCID 1275961—
SolventPyridineHCID 1049—
SolventDiethyl EtherHCID 3283—
ProductN'-t-butyl-N-benzenesulfonyl-N'-benzoylhydrazineHCID 14623289—

Reaction Steps

N'-t-butyl-N'-benzoylhydrazine (0.4 g) was stirred in pyridine (3 ml) at room temperature. Benzenesulfonyl chloride (0.5 g) was added slowly, dropwise and stirred for 2 hours, diluted with diethyl ether (20 ml) and washed several times with a 10% HCl solution and then water. The organic layer was dried over magnesium sulfate, filtered and the solvent rotavapped off to afford a white solid in good yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424333
Source datasetuspto-grants-1995_06
ORD IDord-47782f9b5f06407a89236f994f00b2a5
Source noteuspto-grants-1995_06