(3-Amino-4-methylphenoxy) acetonitrile → (3-Amino-5-chloro-4-methylphenyl) acetonitrile
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:12][C:13]#[N:14])[CH:5]=[C:6]([N+:9]([O-])=O)[C:7]=1[CH3:8].NC1C=C(C=CC=1C)OCC#N.CC1C=CC(OCC#N)=CC=1[N+]([O-])=O>>[NH2:9][C:6]1[CH:5]=[C:4]([CH2:12][C:13]#[N:14])[CH:3]=[C:2]([Cl:1])[C:7]=1[CH3:8]Participants
4
Procedure
(3-Amino-5-chloro-4-methylphenyl) acetonitrile was prepared from (3-chloro-4-methyl-5-nitrophenyl) acetonitrile in a manner similar to that described in Example 2 for the preparation of (3-amino-4-methylphenoxy) acetonitrile from (4-methyl-3-nitrophenoxy) acetonitrile.
Sources & evidence
- ORD record
- ord-258d2d6c98544e9d920ab4dde2e37a2d
- Source dataset
- uspto-grants-1999_09
- Patent number
- US05952362
Reaction notes
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