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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23918Generated: October 26, 2026

1-(3,5-Dioxapiperidin-1-yl)sulphonyl-4-nitrobenzene → 4-(3,5-Dioxapiperidin-1-yl)sulphonylaniline

https://huagongshe.com/reaction/23918

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3,5-Dioxapiperidin-1-yl)sulphonyl-4-nitrobenzeneHCID 22024921—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product4-(3,5-Dioxapiperidin-1-yl)sulphonylanilineHCID 2257022788.9%

Reaction Steps

A mixture of 1-(3,5-dioxapiperidin-1-yl)sulphonyl-4-nitrobenzene (Method 8) (500 mg, 1.82 mmol) and 10% palladium on charcoal catalyst (150 mg) in ethanol (25 ml) and ethyl acetate (25 ml) was stirred under an atmosphere of hydrogen for 3 hours. The catalyst was removed by filtration through diatomaceous earth and the filter pad was washed with ethanol and ethyl acetate. The volatiles were removed from the filtrate by evaporation and the residue triturated with ether and hexane to give the tide compound (395 mg, 88%). NMR: 4.90 (s, 2H) 5.10 (s, 4H), 6.02 (s, 2H), 6.58 (d, 2H), 7.50 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855719B1
Source datasetuspto-grants-2005_02
ORD IDord-ea10996620524120b6e6ff7aa80b2e1c
Source noteuspto-grants-2005_02