戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 7831作成日:2026年10月25日

Butanal → 2-Butyl-5-methoxy-1-indanone

https://huagongshe.com/reaction/7831

反応式

関与物質

役割名称HCID仕込み量
反応物ButanalHCID 261—
反応物Hydrochloric AcidHCID 313—
反応物Potassium HydroxideHCID 14797—
反応物5-Methoxyindan-1-oneHCID 78787—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物2-Butyl-5-methoxy-1-indanoneHCID 1204575253.2%

反応手順

A mixture of 5-methoxy-1-indanone (25.0 g, 154 mmol), 85% KOH (2.03 g, 30.8 mmol), 10% palladium on activated carbon (2 g), and ethanol (150 mL) was placed under a hydrogen atmosphere and stirred while butyraldehyde (16.7 mL, 185 mmol) was added over 2 minutes. The mixture warmed during the addition. The resulting mixture was hydrogenated at room temperature for 3 hours, then filtered to remove the catalyst. The filtrate was acidified with 2N HCl (15.4 mL, 30.8 mmol) and evaporated under vacuum. The residue was partitioned between EtOAc (500 mL) and water (500 mL). The organic phase was washed with water (500 mL) and brine (100 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (33.5 g). The crude product was purified by column chromatography on EM silica gel 60 (230-400 mesh, 670 g), eluting first with CH2Cl2 and then with 5% EtOAc in CH2Cl2, to afford 2-butyl-5-methoxy-1-indanone (17.9 g) 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-81064133f67440459d71cf2f2f14c79e
出典メモuspto-grants-2006_08