Hydrochloric Acid → 3-Allyl-2-norbornanone

Temperature

-20 °C

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%.

1. stirringthe mixture was stirred at -20° C. for 30 minutes
2. temperaturethe temperature of the mixture was raised to room temperature
3. stirringthe mixture was stirred for one hour
4. extractionthe mixture was extracted with toluene (200 ml×4)
5. washThe extract was washed with successive, saturated sodium bicarbonate solution, water, saturated sodium chloride (each 200 ml), and
6. dry with materialdried over anhydrous magnesium sulfate
7. filtrationThe solution was filtered
8. distillationthe solvent was distilled off

ORD record

ord-cee3979477db4382a9a149016f88b502

Source dataset

uspto-grants-1993_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05266728