반응 #95296

ord-55bc0c317f18466394a28c44f3fe2b9e

반응 방정식

B#B
diborane
BrBr
bromine
C#CC(OC1CCCCO1)C(C)(C)CCCC
4,4-dimethyl-3-tetrahydropyranyloxy-1-octyne
CC=C(C)C
2-methyl-2-butene
CCCCC(C)(C)C(/C=C/Br)OC1CCCCO1
title compound
CCCCC(C)(C)C(/C=C/Br)OC1CCCCO1
1-bromo-4,4-dimethyl-3-tetrahydropyranyloxy-trans-1-octene

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the solvent is removed under vacuum
  2. 2
    workup.DISSOLUTIONThe residue is dissolved in 20 ml
  3. 3
    workup.ADDITIONis added a solution of 5.25 g
  4. 4
    기타The cooling bath is removed
  5. 5
    workup.STIRRINGto stir at ambient temperature for 1.5 hours
  6. 6
    온도The mixture is cooled to 0° C.
  7. 7
    기타The cooling bath is removed
  8. 8
    온도the mixture is refluxed for 6 hours under an inert atmosphere
  9. 9
    온도The mixture is cooled
  10. 10
    workup.ADDITIONpoured into dilute sodium hydroxide solution
  11. 11
    세척The organic phase is washed with water and saturated brine
  12. 12
    건조dried (Na2SO4)
  13. 13
    기타evaporated
  14. 14
    기타The 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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04343949uspto-grants-1982_08