Reaktionsgleichung
[CH2:1]([C:5]1[O:6][C:7]2[CH:31]=[CH:30][CH:29]=[CH:28][C:8]=2[C:9]=1[C:10]([C:12]1[CH:17]=[C:16](I)[C:15]([O:19][CH2:20][CH2:21][N:22]([CH2:25][CH3:26])[CH2:23][CH3:24])=[C:14](I)[CH:13]=1)=[O:11])[CH2:2][CH2:3][CH3:4].[BH4-].[Na+]>CO.[Pd](Cl)Cl>[CH2:1]([C:5]1[O:6][C:7]2[CH:31]=[CH:30][CH:29]=[CH:28][C:8]=2[C:9]=1[CH:10]([C:12]1[CH:17]=[CH:16][C:15]([O:19][CH2:20][CH2:21][N:22]([CH2:25][CH3:26])[CH2:23][CH3:24])=[CH:14][CH:13]=1)[OH:11])[CH2:2][CH2:3][CH3:4]Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
One mmole (645 mg) of the ketone, (2-n-butyl-3-benzofuranyl)[4-[2-(diethylamino)ethoxyl]-3,5-diiodophenyl]methanone is dissolved in 10 ml of methanol. Palladium dichloride (2 mmole, 354 mg) is added and the mixture is agitated to suspend the palladium dichloride. The temperature of the mixture is adjusted to 20° C. Sodium borohydride (10 mmole, 379 mg) is added and stirring is continued until reaction is complete (~1 hour). The palladium dichloride is removed by filtration and water is added to the filtrate. An ether extraction is performed and the product is removed from the ether phase by evaporation under reduced pressure. The produce is purified by chromatography (silica gel using methylene chloride) and results in >50% yield of the product, m.p. 203° C. (decomposes).
Aufarbeitung
- customis adjusted to 20° C
- stirringstirring
- customis continued until reaction
- custom(~1 hour)
- customThe palladium dichloride is removed by filtration and water
- additionis added to the filtrate
- extractionAn ether extraction
- customthe product is removed from the ether phase by evaporation under reduced pressure
- customThe produce is purified by chromatography (silica gel using methylene chloride)
Quellen und Nachweise
- ORD-Eintrag
- ord-c69e8fec315d4fc395e287c060e7613c
- Quelldatensatz
- uspto-grants-1989_02
- Patentnummer
- US04806663
Verknüpfte Notizen
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