3,5-Dinitroaniline → 2-[(3,5-Dinitrophenyl)amino]phenylacetic acid

HRID 277273Notes

Reaction equation

HRID 277273 reaction equation
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([OH:11])=[O:10].[N+:12]([C:15]1[CH:16]=[C:17]([CH:19]=[C:20]([N+:22]([O-:24])=[O:23])[CH:21]=1)[NH2:18])([O-:14])=[O:13]>>[N+:12]([C:15]1[CH:16]=[C:17]([NH:18][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2[CH2:8][C:9]([OH:11])=[O:10])[CH:19]=[C:20]([N+:22]([O-:24])=[O:23])[CH:21]=1)([O-:14])=[O:13]

Participants

3

Reactant 2

HCID 120683,5-DinitroanilineHCID 877542-Bromophenylacetic acid

Product 1

HCID 185463882-[(3,5-Dinitrophenyl)amino]phenylacetic acid

Procedure

In the manner described in example 3, 2-bromophenylacetic acid is condensed with 3,5-dinitroaniline to yield 2-[(3,5-dinitrophenyl)amino]phenylacetic acid.

Sources & evidence

ORD record
ord-46d7163b50694bc6bd2e2b5604c9bf46
Source dataset
uspto-grants-2002_03
Patent number
US06355680B1

Reaction notes

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