Ethanol → HCID 70601995, compound

HRID 1973160Notes

Reaction equation

HRID 1973160 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[C:8]2[C:12](=[C:13]([CH3:15])[CH:14]=1)[NH:11][C:10](=S)[CH:9]2C)=[O:5])[CH3:2].C([OH:20])C>[Ni]>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[C:8]2[C:12](=[C:13]([CH3:15])[CH:14]=1)[NH:11][C:10](=[O:20])[CH2:9]2)=[O:5])[CH3:2]

Participants

4

Reactant 2

HCID 702EthanolHCID 86733773HCID 86733773, compound

Product 1

HCID 70601995HCID 70601995, compoundYield 67%

Reagents, catalysts & solvents 1

HCID 935NickelCatalyst

Procedure

An 0.80 g (3.0l mmol) portion of the 5-ethoxycarbonyl-7-methyl-3-methylthio-2-oxindole in 130 ml of absolute ethanol was treated with Raney Nickel by the above described procedure to give 0.44 g (2.0l mmol, 67% yield) of 5-ethoxycarbonyl-7-methyl-2-oxindole, m.p. 238° -241° ;

Sources & evidence

ORD record
ord-110a45407a7d43cab8eb0f612558fb24
Source dataset
uspto-grants-1976_12
Patent number
US03996264

Reaction notes

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