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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 258440Erstellt: 24. Oktober 2026

Hydrochloric Acid → 3-Allyl-2-norbornanone

https://huagongshe.com/de/reaction/258440

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAllyl bromideHCID 7841—
EduktBicyclo(2.2.1)heptan-2-oneHCID 10345—
EduktLithium diisopropylamideHCID 2724682—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelTetrahydrofuran hexaneHCID 21883165—
Produkt3-Allyl-2-norbornanoneHCID 14134638—

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

To 194 ml (388 mmol) of a 2M solution of lithium diisopropyl amide in tetrahydrofuran-hexane, 50 ml of a solution of 38.9 g (353 mmol) of (+)-2-norbornanone in tetrahydrofuran was added dropwise at -40° C., and the mixture was stirred at -20° C. for 30 minutes. Then, 30 ml of a solution of 47.0 g (388 mmol) of allyl bromide in tetrahydrofuran was added dropwise, the mixture was stirred at -20° C. for 30 minutes, the temperature of the mixture was raised to room temperature, and the mixture was stirred for one hour. On ice cooling, the reaction mixture was poured into 300 ml of 2N hydrochloric acid, and the mixture was extracted with toluene (200 ml×4). The extract was washed with successive, saturated sodium bicarbonate solution, water, saturated sodium chloride (each 200 ml), and dried over anhydrous magnesium sulfate. The solution was filtered, and the solvent was distilled off to obtain 77.6 g of crude 3-allyl-2-norbornanone. The crude product was purified by distillation, and 42.5 g (134 mmol) of (+)-exo-3-allyl-2-norbornanone was obtained. Yield: 80%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05266728
Quelldatensatzuspto-grants-1993_11
ORD IDord-cee3979477db4382a9a149016f88b502
Quellennotizuspto-grants-1993_11