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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 966432생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/966432

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참여 물질

역할이름HCID투입량
반응물2-Methyl-2-phenylpropanalHCID 283879—
반응물2,2-Dimethyl-3-phenyloxiraneHCID 5743355—
반응물(S)-4-methylbenzenesulfinamideHCID 11116285—
촉매Titanium tetraethoxideHCID 76524—
촉매Tris(pentafluorophenyl)boraneHCID 582056—
용매BenzeneHCID 241—
생성물(S)-N-(2-Methyl-2-phenylpropylidene)-p-toluenesulfinamideHCID 6962567181%

반응 조건

온도25 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06951955B2
출처 데이터셋uspto-grants-2005_10
ORD IDord-a21d45c9fa064fad827402ad2f202479
출처 메모uspto-grants-2005_10