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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255041Generated: October 30, 2026

N-Methyl-3-nitrobenzenesulfonamide → 3-amino-N-methylbenzenesulfonamide

https://huagongshe.com/reaction/255041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl-3-nitrobenzenesulfonamideHCID 579071—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product3-amino-N-methylbenzenesulfonamideHCID 720489058%

Reaction Steps

A reaction vessel charged with the prepared N-methyl-3-nitro-benzenesulfonamide (4.2 g, 19.42 mmol) in 150 ml of ethyl acetate was further charged with 450 mg of 10% palladium on carbon. The reaction mixture was stirred under hydrogen atmosphere for 48 h, then was filtered through a pad of silica gel washing with EtOAc, and the filtrate was concentrated under reduced pressure. The free base was acidified to give 2.1 g, (˜11 mmol, 58% yield) of the title compound (a compound of formula (W) wherein R is methyl) as its HCl-salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875728B2
Source datasetuspto-grants-2011_01
ORD IDord-b31f7b5e88454c6f98bf455866d30dfb
Source noteuspto-grants-2011_01