Reaktionsgleichung
[OH:1][CH:2]1[CH2:6][CH2:5][CH:4]([CH2:7][CH:8]=O)[CH2:3]1>[Br-].C1([P+](C2C=CC=CC=2)(C2C=CC=CC=2)CCCC)C=CC=CC=1>[CH2:7]([CH:4]1[CH2:5][CH2:6][CH:2]([OH:1])[CH2:3]1)[CH:8]=[CH:6][CH2:2][CH2:3][CH3:4]Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Using the procedure of Example 3, 5 g of 3-hydroxy cyclopentyl-acetaldehyde and 20 g of triphenyl butyl phosphonium bromide were reacted and the product was chromatographed over silica gel. Elution with a 7-3 cyclohexane-ethyl acetate mixture yielded 1.4 g of 3-(2-hexenyl)-cyclopentanol.
Aufarbeitung
- customwere reacted
- customthe product was chromatographed over silica gel
- washElution with a 7-3 cyclohexane-ethyl acetate mixture
Quellen und Nachweise
- ORD-Eintrag
- ord-4cc7bc970b8749cb94668077f684ec93
- Quelldatensatz
- uspto-grants-1985_02
- Patentnummer
- US04501687
Verknüpfte Notizen
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