Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190143Generated: October 31, 2026

N-Methyl-4-nitrobenzeneethanesulfonamide → 4-Amino-N-methylbenzeneethanesulfonamide

https://huagongshe.com/reaction/1190143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl-4-nitrobenzeneethanesulfonamideHCID 13475730—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-Amino-N-methylbenzeneethanesulfonamideHCID 1347576890%

Reaction Steps

A solution of 402 mg (1.65 mmol) of 2-(4-nitro-phenyl)-ethanesulfonic acid methylamide (as prepared in the previous step) in MeOH (30 mL) was hydrogenated over 10% Pd/C (Degussa type E101-NE/W, Aldrich, 50% by weight water) at 20 psi of H2 for 19 h. The reaction mixture was filtered through Celite, and the filter cake was washed with MeOH. Solvents were evaporated in vacuo. Silica gel chromatography of the residue on a 25-g Varian MegaBond Elut SPE column with 50% EtOAc-hexane afforded 318 mg (90%) of the title compound as a white solid: 1H-NMR (CD3CN; 400 MHz): δ 7.01 (d, 2H, J=8.4 Hz), 6.61 (d, 2H, J=8.4 Hz), 5.00-4.92 (br s, 1H), 4.12-4.02 (br s, 2H), 3.24-3.17 (m, 2H), 2.92-2.86 (m, 2H), 2.67 (s, 3H, J=5.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674100B2
Source datasetuspto-grants-2014_03
ORD IDord-bdb16c05c88d4eda9fb9e35434014513
Source noteuspto-grants-2014_03