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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1159695Erstellt: 27. Oktober 2026

Boron trifluoride etherate → 1-(rel-(1R,2S,6S)-6-ethyl-2-methylcyclohex-3-enyl)ethan-1-one

https://huagongshe.com/reaction/1159695

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoron trifluoride etherateHCID 8000—
EduktPotassium CarbonateHCID 11430—
EduktHexen-2-alHCID 12990—
EduktPenta-1,3-dieneHCID 15301—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(rel-(1R,2S,6S)-6-ethyl-2-methylcyclohex-3-enyl)ethan-1-oneHCID 67095432516%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

At −15° C., a solution of BF3.OEt2 (54 g, 0.38 mol) in dichloromethane (680 ml) was treated within 10 min. with 3-hexen-2-one (220.1 g, 89% pure, 2 mol). 1,3-Pentadiene (490 g, 7.2 mol, precooled at 0° C.) was then added and the resulting solution stirred 30 min. at 0° C. then 1 h at 20° C. before being cooled at 0° C. and treated with a solution of 20% aqueous K2CO3 (250 ml). The resulting mixture was stirred 40 min. and concentrated (43° C. till 300 mbar). The aqueous phase was washed with hexane (500 ml) and the combined organic phases with 20% aqueous K2CO3 (100 ml), three times with saturated aqueous NaCl solution, dried (MgSO4) and concentrated. Sulzer-distillation (0.4-0.1 mbar) of the crude product (400 g) gave 1-(rel-(1R,2S,6S)-6-ethyl-2-methylcyclohex-3-enyl)ethan-1-one (326 g, 98% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07812195B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-ffe903658ce043ab98add2185d5c8f9d
Quellennotizuspto-grants-2010_10