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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536041Generated: October 31, 2026

4-Isopropoxy-N-methyl-3-nitrobenzenesulfonamide → 3-amino-N-methyl-4-[(1-methylethyl)oxy]benzenesulfonamide

https://huagongshe.com/reaction/536041

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Isopropoxy-N-methyl-3-nitrobenzenesulfonamideHCID 69935238—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-amino-N-methyl-4-[(1-methylethyl)oxy]benzenesulfonamideHCID 4344929577.6%

Reaction Steps

To a mixture of N-methyl-4-[(1-methylethyl)oxy]-3-nitrobenzenesulfonamide (1.6 g, 5.8 mmol) in ethanol (20 mL) under nitrogen, Pd/C (0.160 g) was added. The flask was then evacuated and recharged with hydrogen three times. The resulting mixture was allowed to stir under a hydrogen atmosphere overnight at room temperature. The mixture was then filtered and concentrated to afford 3-amino-N-methyl-4-[(1-methylethyl)oxy]benzenesulfonamide (1.1 g, 77%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 7.01-7.10 (m, 2H), 6.87-6.98 (m, 2H), 5.08 (br. s., 2H), 4.63 (dt, J=5.93, 11.98 Hz, 1H), 2.34-2.41 (m, 3H), 1.29 (d, J=6.02 Hz, 6H); MS (m/z) 244.7 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859571B2
Source datasetuspto-grants-2014_10
ORD IDord-aa418ae23a0d4180a0fcdf9abd261693
Source noteuspto-grants-2014_10