تفاعل #2028907

ord-049b9a6afd59455d86d9e852754942a8

معادلة التفاعل

Cc1ccccc1
Toluene
CCCC1CCC(C2CCC(c3ccc(-c4ccc(OCC)c(F)c4F)c(F)c3F)C(=O)O2)CC1
3-(4′-ethoxy-2,2′,3,3′-tetrafluorobiphenyl-4-yl)-6-(4-propylcyclohexyl)tetrahydropyran-2-one
Cc1ccccc1
toluene
CC(C)[CH2][Al+][CH2]C(C)C.[H-]
diisobutylaluminum hydride
CCCC1CCC(C2CCC(c3ccc(-c4ccc(OCC)c(F)c4F)c(F)c3F)C(O)O2)CC1
3-(4′-ethoxy-2,2′,3,3′-tetrafluorobiphenyl-4-yl)-6-(4-propylcyclohexyl)tetrahydropyran-2-ol
المردود 99.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىprepared in the ninth step
  2. 2
    أخرىto give two layers
  3. 3
    استخلاصThe water layer was extracted with toluene (20 ml) twice
  4. 4
    غسيلthe combined organic layer was washed with water
  5. 5
    تجفيفdried over anhydrous magnesium sulfate
  6. 6
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure

الإجراء التجريبي

Toluene (20 ml) was added to 3-(4′-ethoxy-2,2′,3,3′-tetrafluorobiphenyl-4-yl)-6-(4-propylcyclohexyl)tetrahydropyran-2-one (11) (2.35 g) prepared in the ninth step. A toluene solution of diisobutylaluminum hydride (0.99 M; 9.6 ml) was added dropwise at −50° C. or lower, and the stirring was continued for 3 hours. The reaction mixture was poured into a 10% aqueous solution of formic acid (50 ml) to give two layers. The water layer was extracted with toluene (20 ml) twice and the combined organic layer was washed with water, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to leave 3-(4′-ethoxy-2,2′,3,3′-tetrafluorobiphenyl-4-yl)-6-(4-propylcyclohexyl)tetrahydropyran-2-ol (12) (2.29 g) in 99% yield.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08389073B2uspto-grants-2013_03