3-Chloro-4-methoxyaniline → HCID 18546375, compound

HRID 277235Notes

Reaction equation

HRID 277235 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].[Cl:12][C:13]1[CH:14]=[C:15]([CH:17]=[CH:18][C:19]=1[O:20][CH3:21])[NH2:16]>>[Cl:12][C:13]1[CH:14]=[C:15]([NH:16][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2[CH2:8][C:9]([OH:11])=[O:10])[CH:17]=[CH:18][C:19]=1[O:20][CH3:21]

Participants

3

Reactant 2

HCID 214413-Chloro-4-methoxyanilineHCID 877542-Bromophenylacetic acid

Product 1

HCID 18546375HCID 18546375, compound

Procedure

In the manner described in example 3, 2-bromophenylacetic acid is condensed with 3-chloro-4-methoxyaniline to yield 2-[(3-chloro-4-methoxyphenyl)amino]phenylacetic acid.

Sources & evidence

ORD record
ord-ff6b60c9d9e84327b2632a0079935083
Source dataset
uspto-grants-2002_03
Patent number
US06355680B1

Reaction notes

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