Allyl 2-methyl-6-nitrobenzoate → Allyl 2-amino-5-chlorobenzoate

HRID 1736365Notes

Reaction equation

HRID 1736365 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N+:14]([O-])=O)=[C:6]([CH:13]=1)[C:7]([O:9][CH2:10][CH:11]=[CH2:12])=[O:8].CC1C=CC=C([N+]([O-])=O)C=1C(OCC=C)=O>>[NH2:14][C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:13][C:6]=1[C:7]([O:9][CH2:10][CH:11]=[CH2:12])=[O:8]

Participants

3

Reactant 2

HCID 19432516Allyl 2-methyl-6-nitrobenzoateHCID 19432544Allyl 5-chloro-2-nitrobenzoate

Product 1

HCID 19432486Allyl 2-amino-5-chlorobenzoate

Procedure

The above nitro compound was reduced by the method described in example 6, for the reduction of allyl 2-methyl-6-nitrobenzoate, to give allyl 2-amino-5-chlorobenzoate.

Sources & evidence

ORD record
ord-5542cc3c3cfd44278e2060f563d62849
Source dataset
uspto-grants-1996_07
Patent number
US05541178

Reaction notes

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