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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194753Generated: November 1, 2026

Hydrochloric Acid → (4-aminophenyl)-N-methylmethylenesulfonamide hydrochloride

https://huagongshe.com/reaction/1194753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-Methyl-1-(4-nitrophenyl)methanesulfonamideHCID 703312—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium monoxideHCID 5083724—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product(4-aminophenyl)-N-methylmethylenesulfonamide hydrochlorideHCID 14234262—

Reaction Steps

A suspension of N-methyl-4-nitrobenzenemethanesulphonamide (30 g) in ethanol (150 ml), water (300 ml) and hydrochloric acid (2N, 65 ml) was hydrogenated over 10% palladium oxide on charcoal (7.5 g, 50% paste with water) until hydrogen uptake ceased (9.75 l). The catalyst was removed by filtration through "hyflo" and the filter pad was washed with water (30 ml). The filtrate was evaporated under reduced pressure to give the title compound as a pale yellow powder (28.2 g) m.p. 143°-144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816470
Source datasetuspto-grants-1989_03
ORD IDord-ccdbfabfb80947ddaf33b139441bf3e6
Source noteuspto-grants-1989_03