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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164412Generated: November 1, 2026

2-(3-Acetylureido)-5-phenoxysulfonylnitrobenzene → 2-(3-Acetylureido)-5-phenoxysulfonylaniline

https://huagongshe.com/reaction/2164412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Acetylureido)-5-phenoxysulfonylnitrobenzeneHCID 15585383—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Solvent2-MethoxyethanolHCID 8019—
Product2-(3-Acetylureido)-5-phenoxysulfonylanilineHCID 15585384—

Reaction Steps

48 g of 2-(3-acetylureido)-5-phenoxysulfonylnitrobenzene in 300 ml of methanol and 300 ml of 2-methoxyethanol are hydrogenated under normal pressure with a catalytic amount of Raney nickel. After hydrogen uptake is complete, the catalyst is filtered off with suction, washed with dimethylformamide and the solution is evaporated under reduced pressure. The residue is stirred with hot methanol, and the solid is filtered off cold under suction and washed with methanol and diisopropyl ether, melting point 202° C., decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04504490
Source datasetuspto-grants-1985_03
ORD IDord-dafcb30e17ad4cb490116da48625e467
Source noteuspto-grants-1985_03