تفاعل #996918

ord-f5ef0617b7bf4da1a8ade7c5d2827804

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىquenched with saturated NH4Cl solution
  2. 2
    استخلاصThe aqueous phase was extracted with ethyl acetate (3×30 ml)
  3. 3
    غسيلThe combined organic phase was washed with brine
  4. 4
    تجفيفdried over anhydrous Na2SO4
  5. 5
    أخرىThe solvent was removed
  6. 6
    أخرىthe residue was purified by flash chromatography on silica gel (Hexane/Ethyl Ether=4:1)

الإجراء التجريبي

(2R)-2-benzhydryl-oxirane (0.5 g, 2.38 mmol) 23a was dissolved in dry THF (5 ml) and was added into a dry THF solution at −78° C. containing CuI (0.045 g, 0.24 mmol) and vinylmagnesium bromide (5.95 ml of 1.0M solution in THF, 5.95 mmol). The reaction mixture was stirred and allowed to reach room temperature over a period of 2 h, and then quenched with saturated NH4Cl solution. The aqueous phase was extracted with ethyl acetate (3×30 ml). The combined organic phase was washed with brine and dried over anhydrous Na2SO4. The solvent was removed and the residue was purified by flash chromatography on silica gel (Hexane/Ethyl Ether=4:1) to give 0.4 g (2S)-1,1-diphenyl-pent-4-ene-2-ol (70%, [α]D=(−)25, c=1, MeOH).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08017791B2uspto-grants-2011_09