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HRID 7828作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/7828

反応式

関与物質

役割名称HCID仕込み量
反応物ButanalHCID 261—
反応物DiisopropylamineHCID 7912—
反応物PentaneHCID 8003—
反応物5-Methoxyindan-1-oneHCID 78787—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2-Butylidene-5-methoxy-1-indanoneHCID 67402813—

反応手順

A solution of diisopropylamine (0.227 mL, 1.62 mmol) in anhydrous tetrahydrofuran (THF, 15 mL) was placed under a nitrogen atmosphere, cooled in an ice bath, and stirred while a 2.0M solution of butyllithium in pentane (0.771 mL, 1.54 mmol) was added dropwise over 2 minutes. The solution was stirred at room temperature for 15 minutes, then cooled in a dry ice-acetone bath and treated dropwise over 3 minutes with a solution of 5-methoxy-1-indanone (250 mg, 1.54 mmol) in THF (2 mL). After stirring at −78° C. for 20 minutes, the reaction mixture was treated with butyraldehyde (0.167 mL, 1.85 mmol). After stirring an additional 26 minutes at −78° C., the reaction mixture was removed from the cooling bath and stirred at room temperature for 90 hours. The reaction mixture was treated with saturated aqueous NH4Cl solution (10 mL) and extracted with EtOAc (15 mL). The organic phase was washed with brine (25 ml), dried over MgSO4, filtered, and evaporated under vacuum to an oil (353 mg). The crude product was purified by silica gel chromatography on a Biotage FLASH 12M column (1.2×15 cm), eluting with 7:1 hexanes-EtOAc, to afford 2-butylidene-5-methoxy-1-indanone (205 mg) as a 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-348e8a54c7c84684b360fbaec8b6e185
出典メモuspto-grants-2006_08