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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723560Generated: October 31, 2026

4-[4-(4-Methoxyphenyl)sulfonylaminomethylbenzyl]-nitrobenzene → 4-[4-(4-Methoxyphenyl)sulfonylaminomethylbenzyl]-phenylamine

https://huagongshe.com/reaction/723560

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[4-(4-Methoxyphenyl)sulfonylaminomethylbenzyl]-nitrobenzeneHCID 21876883—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-[4-(4-Methoxyphenyl)sulfonylaminomethylbenzyl]-phenylamineHCID 6914459487.9%

Reaction Steps

4-[4-(4-Methoxyphenyl)sulfonylaminomethylbenzyl]-nitrobenzene (791 mg) was dissolved in ethyl acetate (15 mL) and hydrogenated over 5% palladium on carbon at room temperature. The reaction was allowed to proceed for 6 hours, filtered, and evaporated to dryness. The crude product thus obtained was chromatographed on a short silica column, eluting with hexane/ethyl acetate (1:1), to give 4-[4-(4-methoxyphenyl)sulfonylaminomethylbenzyl]-phenylamine (645 mg, 87%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141584B2
Source datasetuspto-grants-2006_11
ORD IDord-d555c74325004831af1de400bd456683
Source noteuspto-grants-2006_11