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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 368905생성일: 2026년 10월 25일

tert-Butyl hydroperoxide → (2S,3R)-1,2-Epoxy-2-(2,4-difluorophenyl)butan-3-ol

https://huagongshe.com/reaction/368905

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl hydroperoxideHCID 6410—
반응물Sodium HydroxideHCID 14798—
반응물Sulfuric acid magnesium salt (1:1)HCID 24083—
반응물Diethyl tartrateHCID 6993580—
반응물(2r)-3-(2,4-Difluorophenyl)-3-buten-2-olHCID 11805406—
촉매Titanium isopropoxideHCID 11026—
용매DichloromethaneHCID 6344—
생성물(2S,3R)-1,2-Epoxy-2-(2,4-difluorophenyl)butan-3-olHCID 10867332—

반응 조건

온도-5 °C

반응 단계

To a solution of diethyl L(+)-tartrate (8 ml, 0.047 mole) in dry CH2Cl2 (1.2 L) is added activated 3A° molecular sieve powder (300 g) and cooled the mixture to -5 ° C. Added a solution of titanium (IV) isopropoxide (30 ml, 0.10 mole) followed by t-butyl hydroperoxide (78 ml of 5-6M solution in decane) and continue to stir at -5° C. for 25 minutes. To this mixture, a solution of crude 6b, in CH2Cl2 (100 ml) is added and stirred for 12 hours at 5° C. Cooled the reaction mixture to -40° C., added 70 ml of 30% aq. NaOH solution saturated with NaCI and the mixture is allowed to warm to 10° C. Added 60 g of MgSO4, 20 g of celite and continued to stir at 10° C. for 30 minutes. The mixture is suction-filtered over celite. To the filtrate toluene (1 L), and 700 ml of ether are added and insoluble material removed by filtration. The filtrate is evaporated under reduced pressure to give the crude 7c as a light brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06133485
출처 데이터셋uspto-grants-2000_10
ORD IDord-42cf8306548544bb821ec9a9279510c2
출처 메모uspto-grants-2000_10