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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166470Generated: October 25, 2026

N-(cyclopentyloxy)-3-nitro-1-benzenesulfonamide → 3-amino-N1-(cyclopentyloxy)-1-benzenesulfonamide

https://huagongshe.com/reaction/1166470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(cyclopentyloxy)-3-nitro-1-benzenesulfonamideHCID 22997117—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-amino-N1-(cyclopentyloxy)-1-benzenesulfonamideHCID 22997036100.1%

Reaction Steps

A solution of N-(cyclopentyloxy)-3-nitro-1-benzenesulfonamide (2.98 g, 10.41 mmol) in 50 mL of absolute ethanol was combined with 5 wt % Palladium on barium sulfate (300 mg) and reduced under a balloon of hydrogen gas with vigorous agitation for 18 hours. The mixture was filtered, washed with ethanol, and evaporated in vacuo to a residue. The crude product was purified on flash grade silica gel eluting with 4:1 hexane : ethyl acetate. Fractions containing the product were combined, evaporated in vacuo and dried under vacuum to provide 3-amino-N1-(cyclopentyloxy)-1-benzenesulfonamide (2.67 g, 100%) as an oil. Hl-NMR chloroform-D3): 1.62 (m, 8H), 3.92 (bs, 2H), 4.58 (m, 1H), 6.74 (bs, !H), 6.88 (m, 1H), 7.16 (m, 1H), 7.27 (m, 2H). MS(ESI): 257(MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613743B2
Source datasetuspto-grants-2003_09
ORD IDord-1e2c04737af4416a803144b5ec940e63
Source noteuspto-grants-2003_09