Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605575Generated: November 2, 2026

3-Nitro-4-phenyl-5-sulfamylbenzoic acid → 3-Amino-4-phenyl-5-sulfamylbenzoic acid

https://huagongshe.com/reaction/1605575

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitro-4-phenyl-5-sulfamylbenzoic acidHCID 21546843—
SolventAcetic AcidHCID 176—
SolventPalladiumHCID 23938—
Product3-Amino-4-phenyl-5-sulfamylbenzoic acidHCID 21546841—

Reaction Steps

To a solution of 3-nitro-4-phenyl-5-sulfamylbenzoic acid (8.5 g) in acetic acid (100 ml), palladium (10%) on carbon (1.5 g) is added, and the mixture is hydrogenated. After 2-2.5 hours the theoretical amount of hydrogen has been absorbed, and the hydrogen uptake has subsided. The catalyst is removed by filtration, and the filtrate is evaporated in vacuo. The residue is recrystallized from acetic acid to give 3-amino-4-phenyl-5-sulfamylbenzoic acid with a melting point of 232.5°-237° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03950380
Source datasetuspto-grants-1976_04
ORD IDord-8cf6a0da7ddb42d4960d7d943f93761f
Source noteuspto-grants-1976_04