4-Bromo-2-methylaniline → 4'-Amino-2,3'-dimethylbiphenyl-4-carboxylic acid

HRID 1870890

Reaction equation

HRID 1870890 reaction equation
Br[C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([CH3:9])[CH:3]=1.B([C:13]1[CH:21]=[CH:20][C:16]([C:17]([OH:19])=[O:18])=[CH:15][C:14]=1[CH3:22])(O)O>>[NH2:6][C:5]1[CH:7]=[CH:8][C:2]([C:13]2[CH:21]=[CH:20][C:16]([C:17]([OH:19])=[O:18])=[CH:15][C:14]=2[CH3:22])=[CH:3][C:4]=1[CH3:9]

Participants

3

Reactant 2

HCID 114234-Bromo-2-methylanilineHCID 221158924-Borono-3-methylbenzoic acid

Product 1

HCID 186942714'-Amino-2,3'-dimethylbiphenyl-4-carboxylic acid

Procedure

The title compound was prepared from 4-bromo-2-methylaniline and 4-borono-3-methylbenzoic acid (D29) using a similar procedure to Description 1 as a brown solid (41%). This was used in the next step without further purification.

Workup

  1. customThis was used in the next step without further purification

Sources & evidence

ORD record
ord-3834fa6b35b140f99b470d78d13eaf95
Source dataset
uspto-grants-2000_08
Patent number
US06100272

Linked notes

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