4-Chloro-1-naphthol → 4-Chloro-2-(piperidin-1-yl-o-tolylmethyl)-naphthalen-1-ol
Reaction equation
[Cl-].[CH3:2][C:3]1[CH:15]=[CH:14][CH:13]=[CH:12][C:4]=1[CH:5]=[N+:6]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.[Cl:16][C:17]1[C:26]2[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=2)[C:20]([OH:27])=[CH:19][CH:18]=1>>[Cl:16][C:17]1[C:26]2[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=2)[C:20]([OH:27])=[C:19]([CH:5]([N:6]2[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11]2)[C:4]2[CH:12]=[CH:13][CH:14]=[CH:15][C:3]=2[CH3:2])[CH:18]=1Participants
3
Procedure
The preparation was carried out in accordance with general synthesis instructions 4 from 1-(2-methyl-benzylidene)-piperidinium chloride and 4-chloro-1-naphthol.
Sources & evidence
- ORD record
- ord-a80243adaacb445dbc916b757e1658d1
- Source dataset
- uspto-grants-2007_04
- Patent number
- US07202242B2
Reaction notes
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