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HRID 966432作成日:2026年10月26日

2-Methyl-2-phenylpropanal → (S)-N-(2-Methyl-2-phenylpropylidene)-p-toluenesulfinamide

https://huagongshe.com/reaction/966432

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-2-phenylpropanalHCID 283879—
反応物2,2-Dimethyl-3-phenyloxiraneHCID 5743355—
反応物(S)-4-methylbenzenesulfinamideHCID 11116285—
触媒Titanium tetraethoxideHCID 76524—
触媒Tris(pentafluorophenyl)boraneHCID 582056—
溶媒BenzeneHCID 241—
生成物(S)-N-(2-Methyl-2-phenylpropylidene)-p-toluenesulfinamideHCID 6962567181%

反応条件

温度25 °C

反応手順

To a stirred solution of 2.5 g of 2,2-dimethyl-3-phenyloxirane (16 mmol) in 85 mL of anhydrous benzene is added 0.415 g (0.362 mmol, 5 mol %) of tris(pentafluorophenyl) borane. The light yellow solution is stirred at 25° C. for 19 hours. The reaction mixture containing the 2-methyl-2-phenylpropanal is then treated with (S)-p-toluenesulfinamide (2.3 g, 15 mmol) followed by a solution of 16 mL (73 mmol) titanium ethoxide in 155 mL of benzene. The yellow solution is stirred at 25° C. for 24 hours then cooled to 5-10° C. and quenched with 245 mL of water. The mixture is filtered through diatomaceous earth, and the filter cake washed with methylene chloride (4×50 mL). The aqueous layer is washed with methylene chloride (1×25 mL). The combined organic layers are dried (MgSO4) and concentrated under reduced pressure to give 3.74 g (81%) of the desired product as a white solid. The product is used without further purification in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06951955B2
出典データセットuspto-grants-2005_10
ORD IDord-a21d45c9fa064fad827402ad2f202479
出典メモuspto-grants-2005_10