반응 #639973

ord-5622b7a52f674ac5b0696706191b8fa8

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGThe reaction was stirred for 2 hours
  2. 2
    추출extracted with ethyl acetate (3×50 mL)
  3. 3
    세척The combined organic layers were washed with water, brine
  4. 4
    건조dried over sodium sulfate
  5. 5
    온도cooled to 0° C.
  6. 6
    온도After warming to rt over the course of 1 hour the reaction
  7. 7
    추출The aqueous layer was extracted with ethyl acetate (3×50 mL)
  8. 8
    세척the combined organic layers were washed with water
  9. 9
    건조brine and dried over Na2SO4
  10. 10
    기타Concentration of the solvents under reduced pressure and purification by silica gel

실험 절차

To a solution of (2S,3S)-3-(tert-butoxycarbonyl)-4-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-2-hydroxybutyl acetate (1050 mg, 2603 μmol) in 5 mL of DMF was added 2-methoxypropene (872 μA 9111 μmol) and CSA (181 mg, 781 μmol). The mixture was stirred at rt overnight, and 91 mg of CSA and 0.872 mL of 2-methoxypropene were added. The reaction was stirred for 2 hours, then poured into ice-cold aqueous saturated sodium bicarbonate (150 mL) and extracted with ethyl acetate (3×50 mL). The combined organic layers were washed with water, brine, and dried over sodium sulfate. The derived yellow oil was taken up in 10 mL of methanol cooled to 0° C. and treated with potassium carbonate (1079 mg, 7809 μmol). After warming to rt over the course of 1 hour the reaction was diluted with ethyl acetate (25 mL) and poured in saturated ammonium chloride (50 mL). The aqueous layer was extracted with ethyl acetate (3×50 mL) and the combined organic layers were washed with water and then brine and dried over Na2SO4. Concentration of the solvents under reduced pressure and purification by silica gel provided (4S,5S)-tert-butyl 4-((2,2-difluorobenzo[d][1,3]dioxol-5-yl)methyl)-5-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate as a colorless oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07951838B2uspto-grants-2011_05