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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 520359생성일: 2026년 10월 24일

tert-Butylsulfinamide, (S)-(-)- → (S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoate

https://huagongshe.com/ko/reaction/520359

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butylsulfinamide, (S)-(-)-HCID 11355477—
반응물Ethyl 4-fluoro-3,3-dimethyl-2-oxobutanoateHCID 86690078—
촉매HCID 178477244HCID 178477244—
용매Sodium ChlorideHCID 5234—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoateHCID 8669007930.2%

반응 조건

온도65 °C

반응 단계

To a solution of ethyl 4-fluoro-3,3-dimethyl-2-oxobutanoate (2.3 g, 13.05 mmol) in THF (20 mL) was added (S)-2-methylpropane-2-sulfinamide (1.899 g, 15.67 mmol) and tetraethoxytitanium (5.91 mL, 26.1 mmol). The reaction mixture was heated at 65° C. for 6 h. The reaction mixture was cooled down, diluted with EtOAc and sat. NaCl (40 mL) and stirred at rt for 0.5 h. The solid was filtered and washed with water and EtOAc. The filtrate was separated and the organic layer was washed with water, sat. NaCl, dried (MgSO4) and purified by flash chromatography (EtOAc/hexane) to afford (S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoate (1.1 g). 1H NMR (400 MHz, CDCl3) δ ppm 4.46-4.53 (1H, m), 4.28-4.42 (3H, m), 1.59 (3H, s), 1.21-1.31 (15H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09326973B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-123710cb3b9642a2a1939182945b1418
출처 메모uspto-grants-2016_05