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HRID 368905作成日:2026年10月26日

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

https://huagongshe.com/reaction/368905

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl hydroperoxideHCID 6410—
反応物Sodium HydroxideHCID 14798—
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物Diethyl tartrateHCID 6993580—
反応物(2r)-3-(2,4-Difluorophenyl)-3-buten-2-olHCID 11805406—
触媒Titanium isopropoxideHCID 11026—
溶媒DichloromethaneHCID 6344—
生成物(2S,3R)-1,2-Epoxy-2-(2,4-difluorophenyl)butan-3-olHCID 10867332—

反応条件

温度-5 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06133485
出典データセットuspto-grants-2000_10
ORD IDord-42cf8306548544bb821ec9a9279510c2
出典メモuspto-grants-2000_10