반응 #95296
ord-55bc0c317f18466394a28c44f3fe2b9e
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반응 조건
후처리
- 1기타the solvent is removed under vacuum
- 2workup.DISSOLUTIONThe residue is dissolved in 20 ml
- 3workup.ADDITIONis added a solution of 5.25 g
- 4기타The cooling bath is removed
- 5workup.STIRRINGto stir at ambient temperature for 1.5 hours
- 6온도The mixture is cooled to 0° C.
- 7기타The cooling bath is removed
- 8온도the mixture is refluxed for 6 hours under an inert atmosphere
- 9온도The mixture is cooled
- 10workup.ADDITIONpoured into dilute sodium hydroxide solution
- 11세척The organic phase is washed with water and saturated brine
- 12건조dried (Na2SO4)
- 13기타evaporated
- 14기타The residue is chromatographed upon silica gel
실험 절차
To an ice cooled solution of 3.5 g. (50 moles) of 2-methyl-2-butene in 25 ml. of tetrahydrofuran under an inert atmosphere is added 25 ml. of 1 M diborane in tetrahydrofuran dropwise over 10 minutes. The mixture is stirred at 0°-5° C. for 2 hours and then the solvent is removed under vacuum. The residue is dissolved in 20 ml. of carbon tetrachloride and to the resulting solution cooled to 0° C. is added a solution of 5.25 g. (22 mole) of 4,4-dimethyl-3-tetrahydropyranyloxy-1-octyne (Example 995) in 10 ml. of carbon tetrachloride over 10 minutes. The cooling bath is removed and the mixture is allowed to stir at ambient temperature for 1.5 hours. The mixture is cooled to 0° C. and a solution of 3.52 g. (22 moles) of bromine in 15 ml. of carbon tetrachloride is added over 10 minutes. The cooling bath is removed and the mixture is refluxed for 6 hours under an inert atmosphere. The mixture is cooled and poured into dilute sodium hydroxide solution. The organic phase is washed with water and saturated brine, dried (Na2SO4), and evaporated. The residue is chromatographed upon silica gel and the title compound is isolated with 5% ethyl acetate in benzene.