Реакция #6151

ord-3076d3da99f84c1fb207661fe9054400

Уравнение реакции

CC(C)[CH2][Al+][CH2]C(C)C.[H-]
diisobutylaluminum hydride
CCCCCCCCCCC[C@H](CC(=O)OC(C)(C)C)OC1CCCCO1
t-butyl (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]tetradecanoate
[Cl-].[NH4+]
ammonium chloride
Cl
hydrochloric acid
CCCCCCCCCCC[C@H](CC=O)OC1CCCCO1
(R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]tetradecanal

Растворители

Условия реакции

Температура
-75°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеdid not exceed -70° C
  2. 2
    workup.WAITThe mixture was then left
  3. 3
    Температураto warm to room temperature
  4. 4
    workup.STIRRINGAfter stirring for 1 hour the organic phase
  5. 5
    Другоеwas dried
  6. 6
    Фильтрацияfiltered
  7. 7
    Другоеevaporated
  8. 8
    ДругоеThe material obtained
  9. 9
    Другоеwas chromatographed on silica gel

Методика

I)a) 9.2 g of t-butyl (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]tetradecanoate were dissolved in 115 ml of toluene while gassing with argon and with the exclusion of moisture and cooled to -75° C. 26.5 ml of a 1.2M solution of diisobutylaluminum hydride in toluene were then added dropwise in such a manner that the temperature did not exceed -70° C. After stirring at -75° C. for 1 hour there were added dropwise 7.4 ml of saturated aqueous ammonium chloride solution and subsequently 15.5 ml of 1N hydrochloric acid at -70° C. The mixture was then left to warm to room temperature. After stirring for 1 hour the organic phase was dried, filtered and evaporated. The material obtained was chromatographed on silica gel. There was obtained (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]tetradecanal as a colorless oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05246960uspto-grants-1993_09