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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608165Generated: November 1, 2026

Benzenesulfonyl chloride → N-[2-(furan-2-yl)ethyl]benzenesulfonamide

https://huagongshe.com/reaction/1608165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant2-(Furan-2-yl)ethan-1-amineHCID 1132863—
SolventPyridineHCID 1049—
ProductN-[2-(furan-2-yl)ethyl]benzenesulfonamideHCID 53667225—

Reaction Steps

3.2 g of 2-(2-aminoethyl)-furan are dissolved in 45 ml of pyridine and at 5° C. a solution of 8.8 g of benzenesulphonic acid chloride in 50 ml of pyridine is added. The resulting mixture is then stirred overnight at ambient temperature, the reaction product is evaporated down, the residue is taken up in water and extracted with methylene chloride. After the organic phase has been dried over magnesium sulphate the solution is concentrated by evaporation and chromatographed over a silica gel column using ethylene chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04870076
Source datasetuspto-grants-1989_09
ORD IDord-cf5f3aa3f3474a35a39da982a5f02528
Source noteuspto-grants-1989_09