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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428709Generated: October 27, 2026

N-(4-nitrobenzyl)methanesulfonamide → HCID 12822521, compound

https://huagongshe.com/reaction/1428709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-nitrobenzyl)methanesulfonamideHCID 12822520—
CatalystPalladiumHCID 23938—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 12822521HCID 1282252146%

Reaction Steps

N-(4-Nitrobenzyl)methanesulfonamide (881 mg, 3.83 mmol) was dissolved in methanol/tetrahydrofuran (1:1, 35 mL). 10% Pd/C (264 mg, 3 eq) 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)methanesulfonamide (352 mg, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-3c9ae640203c437e88e89a0d915a67e4
Source noteuspto-grants-2015_01