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HRID 7819作成日:2026年10月24日

Methyl vinyl ketone → 5-Methoxy-2-methyl-2-(3-oxo-butyl)-1-indanone

https://huagongshe.com/ja/reaction/7819

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl vinyl ketoneHCID 6570—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物5-Methoxy-2-methylindan-1-oneHCID 12290490—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物5-Methoxy-2-methyl-2-(3-oxo-butyl)-1-indanoneHCID 21990908332.6%

反応手順

A solution of 5-methoxy-2-methyl-1-indanone (0.5 g, 2.84 mmol) in anhydrous tetrahydrofuran (3 mL) was treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (0.085 mL, 0.57 mmol) and methyl vinyl ketone (0.473 mL, 5.68 mmol). The resulting solution was placed under a nitrogen atmosphere and stirred at room temperature overnight. The mixture was diluted with EtOAc (25 mL), washed with 0.2N HCl (25 mL) and brine (10 mL), dried over MgSO4, filtered, and evaporated under vacuum to a yellow oil (800 mg). The oil was dissolved in CH2Cl2 (10 mL) and the solution added to a small column of EM silica gel 60 (8 mL). The column was eluted with CH2Cl2 (30 ml) and the eluant evaporated under vacuum to afford 5-methoxy-2-methyl-2-(3-oxo-butyl)-1-indanone (467 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-b2f702acf9204650b931ca10badf77fa
出典メモuspto-grants-2006_08