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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1269362생성일: 2026년 10월 26일

Pyridine → 3-({[tert-butyl(dimethyl)silyl]oxy}methyl)phenyl (2Z)-4-hydroxy-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-enyl carbonate

https://huagongshe.com/reaction/1269362

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물TriphosgeneHCID 94429—
반응물3-((((1,1-Dimethylethyl)dimethylsilyl)oxy)methyl)phenolHCID 14940556—
반응물(2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diolHCID 57434773—
용매DichloromethaneHCID 6344—
생성물3-({[tert-butyl(dimethyl)silyl]oxy}methyl)phenyl (2Z)-4-hydroxy-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-enyl carbonateHCID 5884117042.8%

반응 단계

To a solution of 3.06 g of 3-({[tert-butyl(dimethyl)silyl]oxy}methyl)phenol and 1.50 g of triphosgene in 20 mL of CH2Cl2 cooled at −78° C. was added 1.2 mL of pyridine. The reaction mixture was warmed to rt. After 15–30 min, the white suspension was transferred to a solution containing 5.95 g of (2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diol and 1.5 mL of pyridine in 20 mL of CH2Cl2 at rt. The reaction was stirred at rt for 15 min. The reaction was quenched with aqueous 1N HCl, extracted with EtOAc and washed with brine, dried over sodium sulfate, evaporated, and purified by flash chromatography (50–70% EtOAc/hexane) to afford 1.26 g of the title compound as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07199154B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-6194b3a9f7d34c66af83ac79ba135f51
출처 메모uspto-grants-2007_04