Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988080Generated: October 30, 2026

Triethylamine → N-[2-(Aminosulphonyl)4-methoxyphenyl]-4-chlorobutanamide

https://huagongshe.com/reaction/988080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chlorobutyryl chlorideHCID 78370—
Reactant2-Amino-5-methoxybenzenesulfonamideHCID 11252665—
SolventTetrahydrofuranHCID 8028—
ProductN-[2-(Aminosulphonyl)4-methoxyphenyl]-4-chlorobutanamideHCID 15908218—

Reaction Steps

144 mmol of triethylamine are added to a solution containing 96.4 mmol of 2-amino-5-methoxybenzenesulphonamide in 200 ml of tetrahydrofuran (THF), followed dropwise by a solution containing 135 mmol of 4-chlorobutanoic acid chloride in 30 ml of THF. After stirring overnight at room temperature, the THF is removed by evaporation and the residue is taken up in water. After extraction with ethyl acetate, the organic phase is washed and dried. After evaporation, the expected product is obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06635635B2
Source datasetuspto-grants-2003_10
ORD IDord-cd05c004f85e433396a751d84c46e736
Source noteuspto-grants-2003_10