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

HRID 368905

反応式

HRID 368905 の反応式
C([C@@H:6]([C@H:8]([C:10]([O:12][CH2:13]C)=O)[OH:9])O)(OCC)=O.C(OO)(C)(C)C.[F:21][C:22]1[CH:27]=[C:26]([F:28])[CH:25]=[CH:24][C:23]=1C(=C)[C@H](O)C.[OH-].[Na+].[O-]S([O-])(=O)=O.[Mg+2]>C(Cl)Cl.CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-]>[F:21][C:22]1[CH:27]=[C:26]([F:28])[CH:25]=[CH:24][C:23]=1[C@@:10]1([O:12][CH2:13]1)[C@H:8]([OH:9])[CH3:6]

参加物

8

反応条件

温度
-5 °C

実験手順

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.

後処理

  1. stirringstirred for 12 hours at 5° C
  2. temperatureCooled the reaction mixture to -40° C.
  3. temperatureto warm to 10° C
  4. stirringto stir at 10° C. for 30 minutes
  5. filtrationThe mixture is suction-filtered over celite
  6. additionTo the filtrate toluene (1 L), and 700 ml of ether are added
  7. custominsoluble material removed by filtration
  8. customThe filtrate is evaporated under reduced pressure

出典と根拠

ORDレコード
ord-42cf8306548544bb821ec9a9279510c2
出典データセット
uspto-grants-2000_10
特許番号
US06133485

関連ノート

読み込み中…