Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 856115Erstellt: 23. Oktober 2026

2-Pentanone, 5-(acetyloxy)- → 4-Methyl-4-pentenyl acetate

https://huagongshe.com/de/reaction/856115

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Pentanone, 5-(acetyloxy)-HCID 21258—
EduktPotassium tert-butoxideHCID 23665647—
KatalysatorMethyltriphenyliphosphonium bromideHCID 74505—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Methyl-4-pentenyl acetateHCID 1223138560,4%

Reaktionsschritte

Potassium tert-butoxide (9.4 g, 84 mmol) was added to a mixture of methyltriphenylphosphonium bromide (30 g, 84 mmol) in THF (300 ml), and the mixture was stirred at room temperature for 40 minutes. To the mixture a solution of 4-oxopentyl acetate (9.9 g, 68.8 mmol) in THF (30 ml) was gradually added dropwise while cooling in an ice-bath, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was poured into ice water, and extracted with diethyl ether twice. The extracts were combined, washed with brine, and dried over magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=4/1) to afford 4-methyl-4-pentenyl acetate (5.9 g, yield 60.4%) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07262212B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-20fd1cb0da5b437da272849fb0179b44
Quellennotizuspto-grants-2007_08