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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-(cyclopentyloxy)-3-nitro-1-benzenesulfonamide | HCID 22997117 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-amino-N1-(cyclopentyloxy)-1-benzenesulfonamide | HCID 22997036 | 100.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06613743B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-1e2c04737af4416a803144b5ec940e63 |
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| Source note | uspto-grants-2003_09 |
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