N-(4-Bromo-3-chloro-2-methylphenyl)acetamide → 4-Bromo-3-chloro-2-methylaniline

HRID 501562

Reaction equation

HRID 501562 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8]C(=O)C)=[C:4]([CH3:12])[C:3]=1[Cl:13].Cl.NC1C2CCCCC=2C(C#N)=CC=1>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[C:4]([CH3:12])[C:3]=1[Cl:13]

Participants

3

Reactant 2

HCID 86376N-(4-Bromo-3-chloro-2-methylphenyl)acetamideHCID 1317269774-Amino-5,6,7,8-tetrahydronaphthalene-1-carbonitrile, hydrochloride salt

Product 1

HCID 71719114-Bromo-3-chloro-2-methylanilineYield 83%

Procedure

The title compound was prepared (0.70 g, 83% yield) from 22A in a manner similar to that described in Experiment 2D.

Sources & evidence

ORD record
ord-2be1897a6f1b405596aba49a350dfc13
Source dataset
uspto-grants-2010_08
Patent number
US07772267B2

Linked notes

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