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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652033Generated: October 29, 2026

Benzenesulfonamide → 4-[14-(Trimethylsilyl)tetradecylamino]-N-(phenylsulfonyl)benzamide

https://huagongshe.com/reaction/652033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonamideHCID 7370—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium hydrideHCID 24758—
Reactant4-[14-(Trimethylsilyl)tetradecylamino)benzoic acidHCID 13884862—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventDimethylacetamideHCID 31374—
Product4-[14-(Trimethylsilyl)tetradecylamino]-N-(phenylsulfonyl)benzamideHCID 20198315—

Reaction Steps

A solution of 30.7 g. of benzenesulfonamide in 250 ml. of dry dimethylacetamide is added dropwise, with stirring and cooling, to a suspension of 5.4 g. of sodium hydride in 100 ml. of dry dimethylacetamide during 30 minutes at room temperature. Stirring is continued for 30 minutes. In the meantime, a mixture of 36.2 g. of 4-[14-(trimethylsilyl)tetradecylamino] benzoic acid in 100 ml. of methylene chloride, 300 ml. of dimethoxyethane, and 40 ml. of thionyl chloride is refluxed for 1 hour and 15 minutes. The solution is evaporated and to the resulting oil residue is added, in one portion, the previously prepared mixture of sodium benzenesulfonamide in dimethylacetamide. The mixture is stirred for 30 minutes and then filtered. The filtrate is poured into 2 liters of water and 250 ml. of saturated sodium chloride solution. The product is collected by filtration and then dissolved in methylene chloride, the mixture is filtered through diatomaceous earth, and brine is added. The layers are separated, the organic phase is dried and evaporated. The residue is crystallized to yield the product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04670421
Source datasetuspto-grants-1987_06
ORD IDord-27a271ea3bd149c29eff88593d54b0c2
Source noteuspto-grants-1987_06