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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890992Generated: October 30, 2026

Benzenesulfonamide, 3-nitro- → Benzenesulfonamide, 3-amino-

https://huagongshe.com/reaction/1890992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonamide, 3-nitro-HCID 67138—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductBenzenesulfonamide, 3-amino-HCID 737793%

Reaction Steps

3-Nitro-benzenesulfonamide (1.46 g, 7.2 mmol) was hydrogenated over Raney nickel (0.3 g) in methanol at 50° C. and 70 psi for 4 h, then catalyst was filtered out, washed with warm methanol, combined filtrates were evaporated to give 1.15 g (93%) of 3-amino-benzenesulfonamide as colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507498B2
Source datasetuspto-grants-2013_08
ORD IDord-689ce09531954ee4a4b02661edf02b15
Source noteuspto-grants-2013_08