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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164419Generated: November 1, 2026

2-(3-Acetylureido)-5-(3-trifluoromethylphenylsulfonyloxy)nitrobenzene → 2-(3-Acetylureido)-5-(3-trifluoromethylphenylsulfonyloxy)aniline

https://huagongshe.com/reaction/2164419

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Acetylureido)-5-(3-trifluoromethylphenylsulfonyloxy)nitrobenzeneHCID 15585500—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Solvent2-MethoxyethanolHCID 8019—
Product2-(3-Acetylureido)-5-(3-trifluoromethylphenylsulfonyloxy)anilineHCID 15585469—

Reaction Steps

59 g of 2-(3-acetylureido)-5-(3-trifluoromethylphenylsulfonyloxy)nitrobenzene 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 warm 2-methoxyethanol and the solution is evaporated under reduced pressure. Water is added to the residue and it is then filtered off with suction, washed with water and dried over sodium hydroxide, melting point 182° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04504490
Source datasetuspto-grants-1985_03
ORD IDord-9a3d943268f24b79bb1d5b2dca8f26fe
Source noteuspto-grants-1985_03