HCID 21528862, compound → HCID 21528838, compound

HRID 1658223Notes

Reaction equation

HRID 1658223 reaction equation
[CH:1]1([N:7]2[CH2:11][C:10](=[O:12])[N:9]([C:13]3[CH:18]=[CH:17][C:16]([N+:19]([O-])=O)=[CH:15][CH:14]=3)[CH2:8]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1>C(O)C.[Ni]>[CH:1]1([N:7]2[CH2:11][C:10](=[O:12])[N:9]([C:13]3[CH:14]=[CH:15][C:16]([NH2:19])=[CH:17][CH:18]=3)[CH2:8]2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1

Participants

4

Reactant 1

HCID 21528862HCID 21528862, compound

Product 1

HCID 21528838HCID 21528838, compound

Reagents, catalysts & solvents 2

HCID 935NickelCatalystHCID 702EthanolSolvent

Procedure

1-Cyclohexyl-3-(4-nitrophenyl)-imidazolidin-4-one (2.9g) was dissolved in ethanol (500 ml) and 200 mg Raney nickel added. The mixture was then hydrogenated.

Sources & evidence

ORD record
ord-c2f048fa1ebe48f582c99a003b9b13fa
Source dataset
uspto-grants-1976_06
Patent number
US03963706

Reaction notes

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