Reaktionsgleichung
[C:1]1([C:7]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[CH2:10][CH2:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:17](Br)[CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.[CH3:26][Mg]Br.[ClH:29]>C(OCC)C>[ClH:29].[CH3:26][C:7]1([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH2:10][CH2:9][N:8]1[CH2:17][CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
1-Methyl-1-phenyl-2-phenethyl-1,2,3,4-tetrahydroisoquinoline hydrochloride was prepared by reacting 1-phenyl-3,4-dihydroisoquinoline with phenethyl bromide, then 3M diethyl ether solution of methylmagnesium bromide according to a similar manner to that of Example 26, and then converting the resultant compound to its hydrochloride according to a conventional manner.
Quellen und Nachweise
- ORD-Eintrag
- ord-3d18c4b4d53b4219bff15b7851121328
- Quelldatensatz
- uspto-grants-1991_10
- Patentnummer
- US05059608
Verknüpfte Notizen
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