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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1835747Erstellt: 26. Oktober 2026

Allyl bromide → Cyclohexanone, 2-(2-propen-1-yl)-

https://huagongshe.com/reaction/1835747

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktCyclohexanoneHCID 7967—
EduktEthyl AcetateHCID 8857—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTolueneHCID 1140—
ProduktCyclohexanone, 2-(2-propen-1-yl)-HCID 7894471,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Ex-6a) A suspension of potassium t-butoxide (200 g, 1.78 mol) in toluene which was cooled to 0° C. in an ice bath under N2 was treated with cyclohexanone (157 g, 1.60 mol). To the reaction mixture was slowly added allyl bromide (194 g, 1.60 mol) over a 2 hour period. The reaction was warmed to room temperature over 5 hours. The reaction was then poured into EtOAc (400 mL) and washed once with 10% potassium hydrogen sulfate (250 mL). The organic solution was then washed with brine (3×200 mL), dried over magnesium sulfate, and evaporated under reduced pressure. The resulting oil was then chromatographed to yield 158.4 g (71.6%) of 2-allyl cyclohexanone as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06774126B2
Quelldatensatzuspto-grants-2004_08
ORD IDord-584979e462a14ceb968d6a1c9200e159
Quellennotizuspto-grants-2004_08