Reaktionsgleichung
[C:1]1([Bi:7](C2C=CC=CC=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br:20][Bi](Br)Br>C1COCC1>[C:1]1([Bi:7]([Br:20])[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
In 400 ml of THF was dissolved 22.014 g (50 mmol) of triphenylbismuthine (Tokyo Kasei Co., Ltd.) under nitrogen atmosphere. The solution was cooled to 0° C. and thereto was slowly added dropwise 11.231 g (25 mmol) of tribromobismuthine (Aldrich Corp.) (30 minutes). The mixture was stirred to room temperature for 1 hour. The yellow precipitate was filtered and dried in a vacuum. The obtained precipitate was recrystallized from benzene, giving 27.422 g (62 mmol: yield 83%) of yellow powdery product.
Aufarbeitung
- filtrationThe yellow precipitate was filtered
- customdried in a vacuum
- customThe obtained precipitate was recrystallized from benzene
- customgiving 27.422 g (62 mmol: yield 83%) of yellow powdery product
Quellen und Nachweise
- ORD-Eintrag
- ord-6de6a5d0fb9b4c64a493fe578b70f983
- Quelldatensatz
- uspto-grants-2010_12
- Patentnummer
- US07847043B2
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