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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 368905Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/368905

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl hydroperoxideHCID 6410—
EduktSodium HydroxideHCID 14798—
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
EduktDiethyl tartrateHCID 6993580—
Edukt(2r)-3-(2,4-Difluorophenyl)-3-buten-2-olHCID 11805406—
KatalysatorTitanium isopropoxideHCID 11026—
LösungsmittelDichloromethaneHCID 6344—
Produkt(2S,3R)-1,2-Epoxy-2-(2,4-difluorophenyl)butan-3-olHCID 10867332—

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06133485
Quelldatensatzuspto-grants-2000_10
ORD IDord-42cf8306548544bb821ec9a9279510c2
Quellennotizuspto-grants-2000_10