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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164416Generated: November 1, 2026

5-(3-Trifluoromethylphenylsulfonyloxy)-2-ureidonitrobenzene → 5-(3-Trifluoromethylphenylsulfonyloxy)-2-ureidoaniline

https://huagongshe.com/reaction/2164416

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(3-Trifluoromethylphenylsulfonyloxy)-2-ureidonitrobenzeneHCID 15585499—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Solvent2-MethoxyethanolHCID 8019—
Product5-(3-Trifluoromethylphenylsulfonyloxy)-2-ureidoanilineHCID 15585470—

Reaction Steps

61.5 g of 5-(3-trifluoromethylphenylsulfonyloxy)-2-ureidonitrobenzene in 200 ml of methanol and 200 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 methanol and the solution is evaporated under reduced pressure, 1 liter of water is added, and the solid is filtered off with suction, washed with water and dried over NaOH, melting point 172° C., decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04504490
Source datasetuspto-grants-1985_03
ORD IDord-1e69c5487f4b416b91c10fc3e96f5f82
Source noteuspto-grants-1985_03