Реакция #2328978

ord-9907e12207044518ab4d4b3475823ed4

Уравнение реакции

[BH4-].[Na+]
sodium borohydride
C1CCOC1
THF
C=CC1CCC(C2CCC(C=O)CC2)CC1
( 3-3 )
C=CC1CCC(C2CCC(C=O)CC2)CC1
4′-vinylbicyclohexyl-4-carbaldehyde
[Cl-].[NH4+]
ammonium chloride
C=C[C@H]1CC[C@H]([C@H]2CC[C@H](CO)CC2)CC1
trans-4-(trans-4-vinylcyclohexyl)cyclohexylmethanol

Растворители

Условия реакции

Температура
-10°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGwhile stirring the inner temperature
  2. 2
    ТемператураAfter raising the temperature to room temperature
  3. 3
    workup.STIRRINGstirring for 2 hours
  4. 4
    Другоеterminating
  5. 5
    Другоеthe reaction
  6. 6
    workup.ADDITIONThe saturated saline was added to the reacted solution
  7. 7
    Другоеthe organic layer was separated
  8. 8
    Экстракцияthe aqueous layer was extracted with ethyl acetate (twice)
  9. 9
    ПромывкаThe combined organic layer was washed with saturated saline
  10. 10
    Сушкаdried over anhydrous magnesium sulfate
  11. 11
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
  12. 12
    Другоеthe residue was purified by column chromatography

Методика

A THF (180 mL) solution of 60.1 g of a nearly colorless solid obtained in (3-3) was added dropwise in an ethanol (120 mL) solution of 1.65 g of sodium borohydride under stirring at −10° C. while stirring the inner temperature. After raising the temperature to room temperature and stirring for 2 hours, water, ethyl acetate and an aqueous ammonium chloride aqueous were added, thereby terminating the reaction. The saturated saline was added to the reacted solution, and the organic layer was separated, and then the aqueous layer was extracted with ethyl acetate (twice). The combined organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was purified by column chromatography to obtain 15.4 g of trans-4-(trans-4-vinylcyclohexyl)cyclohexylmethanol as a white solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07670504B2uspto-grants-2010_03