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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1269346생성일: 2026년 10월 26일

Imidazole → (2Z)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-en-1-ol

https://huagongshe.com/reaction/1269346

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물(2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diolHCID 57434773—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
용매Sodium chloride; waterHCID 57417360—
생성물(2Z)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-en-1-olHCID 5878778217.5%

반응 조건

온도-78 °C

반응 단계

To a solution of 110 g of (2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diol and 50 g of imidazole in 1 L of THF stirred at −78° C., a solution 51 g of TBSCl in 250 mL of dichloromethane was added dropwise. The resulting mixture was stirred at −78° C. 0.5 hr. Brine was then added and then warmed to room temperature. The organic phase was separated and the aqueous phase was extracted with EtOAc. The organic phases were combined and dried over Na2SO4 and evaporated. The resulting crude material was purified by flash chromatography to afford 25.6 g of the title compound as a white solid. 1H NMR (acetone-d6, 500 M Hz): δ 7.69 (d, 2 H), 7.37 (d, 2 H), 7.18–7.04 (m, 5 H), 4,77 (s, 2 H), 4.65 (d, 2 H), 3.96 (t, 1H, OH), 3.03 (s, 3 H), 0.84 (s, 9 H), 0.01 (s, 6 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07199154B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-bbfc37b0d2ed4f2a81fb6580611a58cd
출처 메모uspto-grants-2007_04