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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481986Generated: October 25, 2026

Triethylamine → Benzenesulfonamide

https://huagongshe.com/reaction/481986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN,N-Bis(2-hydroxyethyl)-4-methylbenzenesulfonamideHCID 81565—
SolventDichloromethaneHCID 6344—
ProductBenzenesulfonamideHCID 737085.7%

Reaction Steps

A solution of 11.4 g (0.1 mole) of methanesulfonyl chloride in 17.1 ml of dichloromethane is cooled to 5° C. A solution of 13 g (0.05 mole) of N,N-bis(2-hydroxyethyl)-4-methylbenzenesulfonamide and 10.1 g (0.1 mole) of triethylamine in 52 ml of dichloromethane is then added dropwise with stirring. The resulting mixture is allowed to return to ambient temperature and stirred for a further 3 hours. The reaction mixture is then extracted three times with 40 ml water. The organic phase is dried over sodium sulfate, filtered and concentrated in a rotating evaporator. The resulting oil is then crystallized from ethanol. 17.8 g of 4-methyl-N,N-bis[2-methylsulfonyloxy)ethyl]benzenesulfonamide are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05792770
Source datasetuspto-grants-1998_08
ORD IDord-ccc72a90f7184e26b8ea2436581a081a
Source noteuspto-grants-1998_08