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HRID 7847作成日:2026年10月25日

Methyl vinyl ketone → 2-Butyl-5-methoxy-4-methyl-2-(3-oxo-butyl)-1-indanone

https://huagongshe.com/reaction/7847

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2-Butyl-5-methoxy-4-methyl-1-indanoneHCID 21990883—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物2-Butyl-5-methoxy-4-methyl-2-(3-oxo-butyl)-1-indanoneHCID 2199089281.4%

反応手順

Methyl vinyl ketone (MVK, 0.49 mL, 5.9 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, 0.12 mL, 0.8 mmol) were added to a solution of impure 2-butyl-5-methoxy-4-methyl-1-indanone (0.90 g, 3.9 mmol) in anhydrous tetrahydrofuran (THF, 3.9 mL). The resulting solution was stirred at room temperature for 30 hours, then diluted with Et2O (50 mL), washed with water (20 mL), 1N HCl (20 mL), and brine (20 mL), dried over MgSO4, filtered, and evaporated under vacuum to an amber oil (1.23 g). The crude product was purified by chromatography on EM silica gel 60 (230-400 mesh, 125 mL dry, packed under 4:1 hexanes-EtOAc). The column was eluted with 4:1 hexanes-EtOAc, collecting 25 mL fractions. Fractions 14-27 gave a 93:2:5 mixture (0.96 g) of 2-butyl-5-methoxy-4-methyl-2-(3-oxo-butyl)-1-indanone, the 6-methyl isomer, and the desmethyl product. This material was used in the next step.

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-2a4993889ca6480cb0bfdfaca22cc970
出典メモuspto-grants-2006_08