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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088721Generated: October 30, 2026

HCID 86643533, compound → (3-Aminophenyl)methanesulfonamide

https://huagongshe.com/reaction/2088721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86643533HCID 86643533—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product(3-Aminophenyl)methanesulfonamideHCID 1326625595%

Reaction Steps

(3-Nitrophenyl)methanesulfonyl amide (3.5 g, 16 mM) was hydrogenated over Raney-Ni (0.5 g) in methanol at 50° C. and 70 psi for 4 hours. Then the catalyst was filtered off and washed with warm methanol. The combined filtrates were evaporated to give 2.83 g (95%) of (3-amino-phenyl)-methanesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436007B2
Source datasetuspto-grants-2013_05
ORD IDord-30eace4a6bf24578a0f9337792d5d3b4
Source noteuspto-grants-2013_05