반응 #304177

ord-78e09dded4224e57bd7945d9535fecad

반응 조건

온도
10°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도After further cooling to 5° C.
  2. 2
    기타to slowly rise to 21-23° C.
  3. 3
    workup.WAITto continue for another hour
  4. 4
    추출extracted with 350 ml n-heptane
  5. 5
    건조The combined organic layers were dried over Na2SO4
  6. 6
    여과After filtration from the desiccant
  7. 7
    기타the solvent was removed in vacuo
  8. 8
    기타The syrupy residue (7.3 g) was purified by flash-chromatography on silica gel employing elution with hexane, hexane/toluene (1:1 mixture), and toluene
  9. 9
    workup.ADDITIONThe fractions containing pure glycidyl-cholesterol (thin layer chromatography (TLC)-monitoring)
  10. 10
    기타dried in vacuo until crystallization

실험 절차

Cholesterol (5.80 g; 15 mmol; Sigma, St. Louis, Mo.) was dissolved in 76 ml dry N,N-dimethylacetamide (DMAc) under a flow of dry argon. The solution was cooled to 10° C. and 15 ml (15 mmol) of a 1.0M solution of lithium tert-butoxide in hexanes (Sigma) was added. After further cooling to 5° C., 10 ml (117 mmol) of freshly distilled epibromohydrin was added and the mixture was stirred at 3-5° C. for 2 hours. The temperature was allowed to slowly rise to 21-23° C. and the reaction was allowed to continue for another hour. The reaction mixture was then diluted with 500 ml of 0.5% aqueous KHCO3 and extracted with 350 ml n-heptane and then twice more with 100 ml n-heptane. The combined organic layers were dried over Na2SO4. After filtration from the desiccant, the solvent was removed in vacuo. The syrupy residue (7.3 g) was purified by flash-chromatography on silica gel employing elution with hexane, hexane/toluene (1:1 mixture), and toluene. The fractions containing pure glycidyl-cholesterol (thin layer chromatography (TLC)-monitoring) were pooled and dried in vacuo until crystallization occurred. The procedure yielded 4.25 g glycidyl-cholesterol (64%). The product displayed an Rf of 0.38 by TLC (silica gel, n-heptane/ethyl acetate, 85:15 by volume). The signals (only those produced by the glycidyl group not present in the starting cholesterol) obtained by 1H NMR analysis of the product are as follows: 2.62 and 2.87 (both m, 1H and 1H, two non-equivalent H of oxirane CH2), 3.15 (m, 1H, CH), and 3.47 and 3.72 (both m, 1H and 1H, diastereotopic H of CH2O).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08193290B2uspto-grants-2012_06