戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 258440作成日:2026年10月26日

Hydrochloric Acid → 3-Allyl-2-norbornanone

https://huagongshe.com/reaction/258440

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Allyl bromideHCID 7841—
反応物Bicyclo(2.2.1)heptan-2-oneHCID 10345—
反応物Lithium diisopropylamideHCID 2724682—
溶媒TetrahydrofuranHCID 8028—
溶媒Tetrahydrofuran hexaneHCID 21883165—
生成物3-Allyl-2-norbornanoneHCID 14134638—

反応条件

温度-20 °C

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05266728
出典データセットuspto-grants-1993_11
ORD IDord-cee3979477db4382a9a149016f88b502
出典メモuspto-grants-1993_11