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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428766Generated: October 26, 2026

N-(4-nitrobenzyl)ethanesulfonamide → N-(4-aminobenzyl)ethanesulfonamide

https://huagongshe.com/reaction/1428766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-nitrobenzyl)ethanesulfonamideHCID 47372696—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-aminobenzyl)ethanesulfonamideHCID 3924342674%

Reaction Steps

N-(4-Nitrobenzyl)ethanesulfonamide (776 mg, 3.18 mmol) was dissolved in methanol and tetrahydrofuran (1:1, 35 mL). 10% Pd/C (264 mg, 3 equiv) was added to it. The resulting mixture was stirred at room temperature for overnight under H2. TLC showed complete consumption of starting material. The mixture was filtered through celite bed and the filterate was concentrated under reduced pressure. The crude was purified by column chromatography to give N-(4-aminobenzyl)ethanesulfonamide (504 mg, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-ff8e9342d21b48bbaee42d5f3ada9961
Source noteuspto-grants-2015_01