Reaktionsgleichung
[CH:1]1([CH:6]([CH2:16][CH3:17])[C:7]([C:9]2[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=2)=[O:8])[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:18][N:19]([CH3:30])[CH2:20][CH2:21][O:22][C:23]1[CH:28]=[CH:27][C:26](Br)=[CH:25][CH:24]=1.Cl>C(O)C>[CH:1]1([CH:6]([CH2:16][CH3:17])[C:7]([C:26]2[CH:27]=[CH:28][C:23]([O:22][CH2:21][CH2:20][N:19]([CH3:30])[CH3:18])=[CH:24][CH:25]=2)([C:9]2[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=2)[OH:8])[CH2:5][CH2:4][CH2:3][CH2:2]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2-cyclopentyl-1-[p-(N,N-dimethyl-2-aminoethoxy)phenyl]-1-(p-hydroxyphenyl)-1-butanol, which was prepared from α-cyclopentyl-p-hydroxybutyrophenone and p-(N,N-dimethyl-2-aminoethoxy) bromobenzene according to the procedure of example 3, was dehydrated in ethanol in the presence of hydrochloric acid. The product was recrystallized from n-hexane, mp. 112°-120° C. and was found to be an 1:1 mixture of E- and Z-isomers.
Aufarbeitung
- customThe product was recrystallized from n-hexane, mp. 112°-120° C.
- additionan 1:1 mixture of E- and Z-isomers
Quellen und Nachweise
- ORD-Eintrag
- ord-4fcd5461932b4ca9abf4342ca40471a3
- Quelldatensatz
- uspto-grants-1985_12
- Patentnummer
- US04556677
Verknüpfte Notizen
Wird geladen…