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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 258444생성일: 2026년 10월 26일

Hydrochloric Acid → 3-Allyl-2-norbornanone

https://huagongshe.com/reaction/258444

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Allyl bromideHCID 7841—
반응물Bicyclo(2.2.1)heptan-2-oneHCID 10345—
반응물Lithium diisopropylamideHCID 2724682—
용매TetrahydrofuranHCID 8028—
용매Tetrahydrofuran hexaneHCID 21883165—
생성물3-Allyl-2-norbornanoneHCID 14134638—

반응 조건

온도-20 °C

반응 단계

To 3.4 ml (6.8 mmol) of a 2M solution of lithium diisopropyl amide in tetrahydrofuran-hexane, 1 ml of a solution of 500 mg (4.54 mmol) of (-)-2-norbornanone in tetrahydrofuran was added dropwise at -40° C., and the mixture was stirred at -20° C. for 10 minutes. Then, 1 ml of a solution of 540 mg (4.46 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 20 ml of 1N hydrochloric acid, and the mixture was extracted with toluene (50 ml×4). The extract was washed with successive, saturated sodium bicarbonate solution, water, saturated sodium chloride (each 50 ml), and dried over anhydrous magnesium sulfate. The solution was filtered, and the solvent was distilled off to obtain 980 mg of crude 3-allyl-2-norbornanone. The product was purified by distillation, and 550 mg (3.66 mmol) of (-)-exo-3-allyl-2-norbornanone was obtained. Yield: 81%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05266728
출처 데이터셋uspto-grants-1993_11
ORD IDord-35e6151db3f24a4a9691d0b55166a66a
출처 메모uspto-grants-1993_11