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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 533538생성일: 2026년 10월 26일

Sodium Sulfite → Ethyl (2R)-4-{4'-[(di-tert-butoxyphosphoryl)oxy]biphenyl-4-yl}-2-methyl-2-(methylsulfonyl)butanoate

https://huagongshe.com/reaction/533538

반응식

참여 물질

역할이름HCID투입량
반응물Sodium SulfiteHCID 24437—
반응물Di-tert-butyl N,N-DiisopropylphosphoramiditeHCID 853005—
반응물Ethyl (2R)-4-(4'-hydroxybiphenyl-4-yl)-2-methyl-2-(methylsulfonyl)butanoateHCID 66579462—
반응물HCID 178418441HCID 178418441—
용매TetrahydrofuranHCID 8028—
생성물Ethyl (2R)-4-{4'-[(di-tert-butoxyphosphoryl)oxy]biphenyl-4-yl}-2-methyl-2-(methylsulfonyl)butanoateHCID 6657787091%

반응 단계

A solution of 1H-tetrazole (2.37 g, 33.9 mmol, 3.0 equiv), di-tert-butyl-N,N-diisopropylphosphoramidite (7.42 mL, 22.6 mmol, 2.0 equiv), and ethyl(2R)-4-(4′-hydroxybiphenyl-4-yl)-2-methyl-2-(methylsulfonyl)butanoate (4.25 g, 11.3 mmol, 1.0 equiv) in tetrahydrofuran (113 mL) was allowed to stir overnight at room temperature. A solution of saturated sodium sulfite (330 mL) was added, and the mixture was extracted with dichloromethane (3×440 mL). The combined organic layers were washed with water (3×330 mL), brine (3×330 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude material was purified by flash chromatography on silica gel (50% ethyl acetate in heptane) to provide a colorless oil (5.84 g, 91%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.33 (t, J=7.13 Hz, 3H) 1.50-1.52 (m, 18H) 1.71 (s, 3H) 2.17-2.30 (m, 1H) 2.46-2.61 (m, 2H) 2.72-2.85 (m, 1H) 3.04 (s, 3H) 4.26 (qd, J=7.13, 1.27 Hz, 2H) 7.21-7.28 (m, 4H) 7.45-7.53 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853258B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-be947402c8f94724b7e6e7a24b3b420b
출처 메모uspto-grants-2014_10