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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841951Generated: October 26, 2026

Ethanol → Benzenesulfonamide, 4-amino-N-[2-(4-morpholinyl)ethyl]-

https://huagongshe.com/reaction/1841951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantAmmonium ChlorideHCID 25517—
ReactantN-(2-Morpholin-4-yl-ethyl)-4-nitro-benzenesulfonamideHCID 743362—
CatalystIronHCID 23925—
SolventWaterHCID 962—
ProductBenzenesulfonamide, 4-amino-N-[2-(4-morpholinyl)ethyl]-HCID 12056978%

Reaction Steps

N-(2-Morpholin-4-yl-ethyl)-4-nitro-benzenesulfonamide (0.14 g, 0.45 mmol) was suspended in a 5:1 mixture of ethanol and water (3 ml). To this solution was added iron powder (0.13 g, 2.25 mmol) followed by saturated ammonium chloride solution (0.1 ml) and the mixture was stirred at room temperature for 18 hours. After this time, the reaction mixture was filtered through a pad of celite, the celite was washed with ethanol (10 ml) and ethyl acetate (50 ml) and the solution was concentrated under vacuum. The resulting residue was partitioned between DCM (50 ml) and water (20 ml), the organic layer was separated, dried with MgSO4, filtered and concentrated to afford the title compound (0.1 g, 78% yield) as a brown solid. Tr=0.35 min, m/z (ES+) (M+H)+ 285.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946197B2
Source datasetuspto-grants-2015_02
ORD IDord-4ac684ae0b794e45a27c19eac27c0c9e
Source noteuspto-grants-2015_02