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HRID 229894作成日:2026年10月25日

Benzaldehyde → alpha-Vinylbenzyl alcohol

https://huagongshe.com/reaction/229894

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物VinyltrimethoxysilaneHCID 76004—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物4,4'-Bi-1,3-benzodioxole-5,5'-diylbis{bis[4-methoxy-3,5-bis(2-methyl-2-propanyl)phenyl]phosphine}HCID 11194192—
反応物Triethoxysilane fluorideHCID 131727541—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物alpha-Vinylbenzyl alcoholHCID 9298665%

反応条件

温度40 °C

反応手順

To a DMF (0.3 mL) solution of Cu(O-Bu-t) (20 mg, 0.02 mmol) as synthesized according to the method described in the publication Inorg. Chim. Acta, 1981, 20, 2728, (R)-DTBM-SEGPHOS (35 mg, 0.03 mmol) and triethoxysilane fluoride (4.0 μL, 0.02 mmol), 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 40° C., and the mixture was stirred for 30 minutes. 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 as an (S)-form in a yield of 65% and an optical purity of 94% ee.

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-3353b18e57c44e9185ae97fa46807060
出典メモuspto-grants-2009_07