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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 368901Erstellt: 23. Oktober 2026

Sodium Chloride → (1S)-[(2R)-(2,4-difluorophenyl)-2-oxiranyl]ethanol

https://huagongshe.com/de/reaction/368901

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
Edukttert-Butyl hydroperoxideHCID 6410—
EduktSodium HydroxideHCID 14798—
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
EduktDiethyl tartrateHCID 6993580—
Edukt(2S)-3-(2,4-Difluorophenyl)-3-buten-2-olHCID 15130435—
KatalysatorTitanium isopropoxideHCID 11026—
LösungsmittelDichloromethaneHCID 6344—
Produkt(1S)-[(2R)-(2,4-difluorophenyl)-2-oxiranyl]ethanolHCID 10631861393,3%

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

To a solution of diethyl L(+)-tartrate (161 ml, 0.94 mole) in dry CH2Cl2 (24 L) was added activated 3A° molecular sieve powder (600 g) and cooled the mixture to -5° C. Added a solution of titanium (IV) isopropoxide (597 ml, 2.0 mole) followed by t-butyl hydroperoxide (1.56 L of 5-6M solution in decane) and continue to stir at -5° C. for 25 minutes. To this mixture, a solution of crude 6a, (664 g) in CH2Cl2 (2 L) was added and stirred for 12 hours at 5° C. Cooled the reaction mixture to -40° C., added 1.4 L of 30% aq. NaOH solution saturated with NaCl and the mixture was allowed to warm to 10° C. Added 1.2 kg of MgSO4, 400 g of celite and continued to stir at 10° C. for 30 minutes. The mixture was suction-filtered over celite. To the filtrate toluene (20 L), and 15 L of ether were added and insoluble material removed by filtration. The filtrate was evaporated under reduced pressure to give the crude 7a as a light brown oil (740 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06133485
Quelldatensatzuspto-grants-2000_10
ORD IDord-007c59cd1045405dba9cea606c3c1507
Quellennotizuspto-grants-2000_10