تفاعل #6151

ord-3076d3da99f84c1fb207661fe9054400

معادلة التفاعل

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

المذيبات

ظروف التفاعل

درجة الحرارة
-75°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىdid not exceed -70° C
  2. 2
    workup.WAITThe mixture was then left
  3. 3
    درجة الحرارةto warm to room temperature
  4. 4
    workup.STIRRINGAfter stirring for 1 hour the organic phase
  5. 5
    أخرىwas dried
  6. 6
    ترشيحfiltered
  7. 7
    أخرىevaporated
  8. 8
    أخرىThe material obtained
  9. 9
    أخرىwas chromatographed on silica gel

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05246960uspto-grants-1993_09