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HRID 7825作成日:2026年10月24日

2-Butyl-5-methoxy-2-(3-oxo-pentyl)-1-indanone → 9a-butyl-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one

https://huagongshe.com/ja/reaction/7825

反応式

関与物質

役割名称HCID仕込み量
反応物2-Butyl-5-methoxy-2-(3-oxo-pentyl)-1-indanoneHCID 21990927—
溶媒Acetic AcidHCID 176—
溶媒Hydrochloric AcidHCID 313—
生成物9a-butyl-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 1204577595.4%

反応条件

温度100 °C

反応手順

A solution of 2-butyl-5-methoxy-2-(3-oxo-pentyl)-1-indanone (84 mg, 0.28 mmol) in acetic acid (0.5 mL) and 6N HCl (0.5 mL) was stirred and heated in an oil bath at 100° C. for 21 hours. After cooling to room temperature, the reaction mixture was partitioned between EtOAc (20 mL) and water (20 mL). The organic phase was washed with water (10 mL), 5% NaHCO3 (20 mL), and brine (10 mL), dried over MgSO4, filtered, and evaporated under vacuum to afford 9a-butyl-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (76 mg) as a gum.

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-13b6e50ba0aa46dbbb22df4807534675
出典メモuspto-grants-2006_08