HCID 19432528, compound → HCID 18780396, compound

HRID 1736370Notes

Reaction equation

HRID 1736370 reaction equation
[CH2:1]([O:4][C:5]([C:7]1[C:8]([N+:19]([O-])=O)=[C:9]([CH:16]=[CH:17][CH:18]=1)[C:10]([O:12][CH2:13][CH:14]=[CH2:15])=[O:11])=[O:6])[CH:2]=[CH2:3]>C(O)C>[CH2:1]([O:4][C:5]([C:7]1[C:8]([NH2:19])=[C:9]([CH:16]=[CH:17][CH:18]=1)[C:10]([O:12][CH2:13][CH:14]=[CH2:15])=[O:11])=[O:6])[CH:2]=[CH2:3]

Participants

3

Reactant 1

HCID 19432528HCID 19432528, compound

Product 1

HCID 18780396HCID 18780396, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

The above nitro compound was reduced by the method described in example 6, except that the solvent was ethanol, to give allyl 3-allyloxycarbonyl-2-aminobenzoate.

Sources & evidence

ORD record
ord-6a885ab6f4314663bb46ec5c456aecaa
Source dataset
uspto-grants-1996_07
Patent number
US05541178

Reaction notes

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