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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428739Generated: October 29, 2026

N-(2-fluoro-4-nitrobenzyl)methanesulfonamide → N-(4-amino-2-fluorobenzyl)methanesulfonamide

https://huagongshe.com/reaction/1428739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-fluoro-4-nitrobenzyl)methanesulfonamideHCID 86679366—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-amino-2-fluorobenzyl)methanesulfonamideHCID 8667936786.5%

Reaction Steps

To a stirred solution of N-(2-fluoro-4-nitrobenzyl)methanesulfonamide (250 mg, 1.007 mmol) in tetrahydrofuran and ethanol as co-solvent were added 10% Pd/C (25 mg). The mixture was charged with H2 (gas) balloon. The resulting mixture was stirred for 15 h, then filtered by using celite. The filtrate was removed in vacuo. The crude was purified by column chromatography. N-(4-Amino-2-fluorobenzyl)methanesulfonamide (190 mg) was obtained as 86% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-17862222d0ab44c58a5ceb989df33303
Source noteuspto-grants-2015_01