Dimethylamine → 2-(4-chlorophenoxy)-N,N-dimethylethanamine
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:9][CH2:10]Br)=[CH:4][CH:3]=1.[CH3:12][NH:13][CH3:14]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:9][CH2:10][N:13]([CH3:14])[CH3:12])=[CH:4][CH:3]=1Participants
3
Procedure
The title compound was prepared in 61% yield (26% SM recovered) by essentially following the procedure outlined in Example 34, Part A from 2-bromoethyl 4-chlorophenyl ether and dimethylamine.
Sources & evidence
- ORD record
- ord-d93b0bef1d9447c191f0b4a4eac5178f
- Source dataset
- uspto-grants-2001_07
- Patent number
- US06265575B1
Reaction notes
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