戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 7848作成日:2026年10月24日

Acetic Acid → 9a-butyl-7-methoxy-8-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one

https://huagongshe.com/ja/reaction/7848

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物PyrrolidineHCID 31268—
反応物2-Butyl-5-methoxy-4-methyl-2-(3-oxo-butyl)-1-indanoneHCID 21990892—
溶媒TolueneHCID 1140—
溶媒Diethyl EtherHCID 3283—
生成物9a-butyl-7-methoxy-8-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 2199088455.5%

反応条件

温度80 °C

反応手順

A solution of impure 2-butyl-5-methoxy-4-methyl-2-(3-oxo-butyl)-1-indanone (0.96 g, 3.17 mmol), acetic acid (0.182 mL, 3.18 mmol) and pyrrolidine (0.265 mL, 3.18 mmol) in anhydrous toluene (15.9 mL) was stirred and heated in an oil bath at 80° C. for 16 hours. After cooling, the reaction mixture was diluted with Et2O (100 mL), washed with 1N HCl (2×25 mL), 5% NaHCO3 (50 mL), and brine (50 mL), dried over MgSO4, filtered, and evaporated under vacuum to a dark brown oil (0.86 g). The crude product was purified by chromatography on a Biotage FLASH 40S column, eluting with 9:1 hexanes-EtOAc, to afford 9a-butyl-7-methoxy-8-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (0.50 g) as an off-white solid.

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-c4d098d6e0c64655809c3a2af90167be
出典メモuspto-grants-2006_08