반응 #70360

ord-aa3587debb534b9981fb9191b6c31d62

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도at reflux for 8 h
  2. 2
    온도The suspension was cooled with an ice bath
  3. 3
    기타quenched by careful addition of H2O (1 mL) and 4N NaOH (0.20 mL)
  4. 4
    여과The mixture was filtered through a Celite pad
  5. 5
    세척the filter cake was washed with THF (3×10 mL)
  6. 6
    건조The filtrate was dried over Na2SO4
  7. 7
    기타evaporated to dryness
  8. 8
    기타the residue was purified by flash chromatography (SiO2, n-hexane/CH2Cl2/acetone 40/30/30)

실험 절차

To a stirred suspension of LiAlH4 (0.247 mg) in THF under N2 (10.5 mL), a solution of 3β-hydroxy-5α,6α-epoxyandrostane-17-one (0.64 g) in THF (20 mL) was added dropwise and the mixture was stirred at reflux for 8 h. The suspension was cooled with an ice bath and then quenched by careful addition of H2O (1 mL) and 4N NaOH (0.20 mL). The mixture was filtered through a Celite pad and the filter cake was washed with THF (3×10 mL). The filtrate was dried over Na2SO4, evaporated to dryness and the residue was purified by flash chromatography (SiO2, n-hexane/CH2Cl2/acetone 40/30/30) to give androstane-3β,5α,17β-triol (0.48 g, 74%). 1H-NMR (300 MHz, DMSO-d6, ppm from TMS): δ 4.37 (1H, d), 4.19 (1H, d), 3.78 (1H, m), 3.62 (1H, s), 3.39 (1H, m), 1.87-0.80 (21H, m), 0.86 (3H, s), 0.59 (3H, s).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08536160B2uspto-grants-2013_09