Phenethylamine → 1-Methyl-1,2,3,4-tetrahydroisoquinoline
Reaction equation
[CH2:1]([NH2:9])[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:10](Cl)(=O)[CH3:11]>>[CH3:10][CH:11]1[C:8]2[C:3](=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH2:2][CH2:1][NH:9]1Participants
3
Procedure
In accordance with the same procedures as in Steps 1, 2, and 3 of Preparation 21, except for using phenethylamine and acetyl chloride, 1-methyl-1,2,3,4-tetrahydroisoquinoline was obtained. In accordance with the same procedures as in Preparation 20, the titled compound was obtained as pale yellow oil. (Yield: 91%) The product was used in the subsequent step without further purification.
Workup
- customIn accordance with the same procedures as in Steps 1, 2, and 3 of Preparation 21
Sources & evidence
- ORD record
- ord-343c910ec416436ebb2ad3a46772e92c
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08188114B2
Reaction notes
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