Heptyltriphenylphosphonium bromide → (Z)-2-Methyl-2-[1-(1-octenyl)cyclopropyl]-1,3-dioxolan

HRID 1790892

Reaktionsgleichung

[Br-].[CH2:2]([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH3:28][C:29]1([C:34]2([CH:37]=O)[CH2:36][CH2:35]2)[O:33][CH2:32][CH2:31][O:30]1>>[CH3:28][C:29]1([C:34]2(/[CH:37]=[CH:2]\[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[CH2:36][CH2:35]2)[O:33][CH2:32][CH2:31][O:30]1

Komponenten

Edukt 2

HCID 2724567Heptyltriphenylphosphonium bromide

HCID 143755571-(2-Methyl-1,3-dioxolan-2-YL)cyclopropane-1-carbaldehyde

Produkt 1

HCID 69650424(Z)-2-Methyl-2-[1-(1-octenyl)cyclopropyl]-1,3-dioxolan

Versuchsvorschrift

4.87 g of heptyltriphenylphosphonium bromide and 1.25 g of aldehyde 7 are reacted analogously to 193., and 978 mg of title substance 206 is obtained as a colorless oil (only Z-isomer).

Aufarbeitung

custom, and 978 mg of title substance 206 is obtained as a colorless oil (only Z-isomer)

Quellen und Nachweise

ORD-Eintrag: ord-72ef0d959b81425ab540df2aa60f8e0a
Quelldatensatz: uspto-grants-2006_07
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US07071344B1

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