Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072692Generated: November 3, 2026

Ammonium Hydroxide → 4-(4-Methoxybenzoyl)thiophene-2-sulfonamide

https://huagongshe.com/reaction/2072692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantThionyl ChlorideHCID 24386—
Reactant4-(4-Methoxybenzoyl)thiophene-2-sulfonic acidHCID 14639067—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
Product4-(4-Methoxybenzoyl)thiophene-2-sulfonamideHCID 14639069—

Reaction Steps

To 2.98 g (0.01 mol) of product from Step B suspended in 75 ml CH2Cl2 was added excess thionyl chloride and the resulting suspension was stirred, and heated at reflux for 1.5 hours to give a homogeneous solution. The thionyl chloride was evaporated and the residue was extracted with CHCl3 after ice had been added. The organic extract was washed with brine, dried and the solvent evaporated to give a yellow oil. This was taken up in acetone and treated with 5 ml of concentrated NH4OH dropwise. After stirring for 15 minutes, this was extracted with chloroform and the extract was dried. Filtration and evaporation of the solvent gave the desired product as a yellow solid, m.p. 173°-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914111
Source datasetuspto-grants-1990_04
ORD IDord-2ac3e362dc4d42f38ee2385855534612
Source noteuspto-grants-1990_04