戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 7877作成日:2026年10月24日

Hydrochloric Acid → 2-[2-(2-Ethyl-[1,3]dioxolan-2-yl)-ethyl]-5-methoxy-3-propyl-1-indanone

https://huagongshe.com/ja/reaction/7877

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Potassium HydroxideHCID 14797—
反応物2-(2-Ethyl-1,3-dioxolan-2-yl)acetaldehydeHCID 13489223—
反応物5-Methoxy-3-propyl-1-indanoneHCID 21990859—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物2-[2-(2-Ethyl-[1,3]dioxolan-2-yl)-ethyl]-5-methoxy-3-propyl-1-indanoneHCID 2199085329.1%

反応手順

A mixture of 5-methoxy-3-propyl-1-indanone (184 mg, 0.90 mmol) and (2-ethyl-[1,3]dioxolan-2-yl)acetaldehyde (173 mg, 1.20 mmol) was treated with a solution of KOH (85% wt. pure, 20 mg, 0.30 mmol) in ethanol (1.0 mL). The resulting mixture was stirred at room temperature for 30 minutes, then treated with 10% Pd on carbon (9 mg), placed under a hydrogen atmosphere, and stirred vigorously at room temperature for 18 hours. The mixture was acidified with 2N HCl and partitioned between EtOAc (9 mL) and water (5 mL). The organic phase was washed with brine, dried over MgSO4, filtered, and evaporated under vacuum to an oil (316 mg). The crude product was purified by chromatography on a Biotage FLASH 12M column, eluting with 10% EtOAc in hexanes, to afford 2-[2-(2-ethyl-[1,3]dioxolan-2-yl)-ethyl]-5-methoxy-3-propyl-1-indanone (87 mg) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087599B2
出典データセットuspto-grants-2006_08
ORD IDord-61d811177b4e4cd88b1e29266c8ae876
出典メモuspto-grants-2006_08