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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1629797생성일: 2026년 10월 25일

Water → (NZ)-N-[1-(4-butoxyphenyl)ethylidene]-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/1629797

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ethanone, 1-(4-butoxyphenyl)-HCID 79814—
반응물Tert-ButanesulfinamideHCID 3382465—
촉매HCID 178477244HCID 178477244—
용매TetrahydrofuranHCID 8028—
생성물(NZ)-N-[1-(4-butoxyphenyl)ethylidene]-2-methylpropane-2-sulfinamideHCID 8959947987%

반응 조건

온도70 °C

반응 단계

To a stirred solution of 1-(4-butoxyphenyl)ethanone (3 g, 15.60 mmol) and 2-methylpropane-2-sulfinamide (2.84 g, 23.41 mmol) in THF (50 mL) was added tetraethoxytitanium (8.90 g, 39.0 mmol). The reaction was heated to 70° C. for 3 d. Cold water was added and the reaction was stirred vigorously for 20 min. The mixture was filtered through Celite® and the filtrated was diluted with EtOAc. The organic solution was washed with H2O, brine, dried over MgSO4, filtered and concentrated. The crude product was by silica gel chromatography (220 g silica gel, eluted with EtOAc in hexanes) to yield the desired product (4 g, 87%) as a yellow oil. 1H NMR (500 MHz, CDCl3) δ 7.88 (d, J=8.80 Hz, 2H), 6.91 (d, J=8.80 Hz, 2H), 4.02 (t, J=6.46 Hz, 2H), 2.73 (s, 3H), 1.75-1.83 (m, 2H), 1.46-1.56 (m, 2H), 1.32 (s, 9H), 0.99 (t, J=7.43 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08791091B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-a983141af41d4b7fa0dbce83c168b1d6
출처 메모uspto-grants-2014_07