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HRID 229892作成日:2026年10月25日

Benzaldehyde → alpha-Vinylbenzyl alcohol

https://huagongshe.com/reaction/229892

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物DimethylformamideHCID 6228—
反応物VinyltrimethoxysilaneHCID 76004—
反応物Tetrabutylammonium FluorideHCID 2724141—
触媒Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
溶媒WaterHCID 962—
生成物alpha-Vinylbenzyl alcoholHCID 92986100%

反応条件

温度60 °C

反応手順

To a DMF (0.2 mL) solution of CuF.3PPh3.2EtOH (10 mg, 0.01 mmol) as synthesized according to the method described in the foregoing publication and dppf (8 mg, 0.014 mmol) (this catalyst preparation method is designated as “A”; hereinafter the same), benzaldehyde (0.020 mL, 0.20 mmol) and vinyltrimethoxysilane (62 μL, 0.40 mmol) were added at room temperature under an argon atmosphere, the temperature was then raised to 60° C., and the mixture was stirred for 3 hours. Thereafter, the reaction mixture was allowed to stand for cooling to room temperature, to which was then added tetrabutylammonium fluoride (TBAF) (1M/THF, 0.5 mL), and the mixture was stirred for 10 minutes. After adding water, the mixture was extracted with ethyl acetate, and the resulting organic layer was washed with saturated brine and then dried over anhydrous sodium sulfate. After drying, the solvent was distilled off, and the residue was subjected to silica gel column chromatography (ethyl acetate/hexane: 1/9 to 1/4), thereby obtaining desired 1-phenyl-2-propen-1-ol in a yield of 100%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07563916B2
出典データセットuspto-grants-2009_07
ORD IDord-2267b6e46bd944d09f0bfeb09e8cd56d
出典メモuspto-grants-2009_07