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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224531Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 3856345, compound

https://huagongshe.com/reaction/224531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
ReactantCumylamineHCID 68509—
ReactantHCID 22164290HCID 22164290—
ProductHCID 3856345HCID 385634567%

Reaction Steps

The N-(α,α-dimethylbenzyl)benzenesulfonamide used as a starting compound in the above procedure could be prepared in the following manner. A two-layered mixture consisting of 33.8 g (0.25 mole) of α,α-dimethylbenzylamine and 120 ml of a 10% aqueous solution of sodium hydroxide was stirred at below 40° C., and 44.1 g of benzenesulfonyl chloride was added dropwise. Stirring the mixture for an additional 1.5 hours afforded a white precipitate. The solid precipitate was collected by filtration, and recrystallized from methanol to afford N-(α,α-dimethylbenzyl)benzenesulfonamide having melting point of 114° to 115° C. in a yield of 67%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04233061
Source datasetuspto-grants-1980_11
ORD IDord-2ecfb2d865554aabbca384edde436de7
Source noteuspto-grants-1980_11