반응 #1403

ord-d4e2b55500174bc5b7869b5b5174c913

반응 방정식

[Li][CH2]CCC
n-Butyllithium
C#C[Si](C)(C)C
trimethylsilylacetylene
[CH3][Al+][CH3].[Cl-]
dimethylaluminum chloride
COc1ccc(C2=CC(=O)CCC2)cc1OC1CCCC1
3-(3-cyclopentyloxy-4-methoxyphenyl)cyclohex-2-en-1-one
[Al+3].[Al+3].[C-]#[C-].[C-]#[C-].[C-]#[C-]
aluminum acetylide
Cl
HCl
O=P([O-])([O-])[O-].[K+].[K+].[K+]
potassium phosphate
CC(C)[CH2][Al+][CH2]C(C)C.[H-]
diisobutylaluminum hydride
COc1ccc(C2(C#C[Si](C)(C)C)CCCC(=O)C2)cc1OC1CCCC1
3-(3-cyclopentyloxy-4-methoxyphenyl)-3-trimethylsilylethynyl cyclohexan-1-one

반응 조건

온도
-10°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITAfter 3.5 h at room temperature
  2. 2
    여과the mixture was filtered through Celite® under an argon atmosphere
  3. 3
    workup.WAITAfter 10 min
  4. 4
    workup.ADDITIONwas added dropwise over 20 min
  5. 5
    workup.WAITAfter 18 h at room temperature
  6. 6
    추출the aqueous layer was extracted twice with ether
  7. 7
    추출The combined extract
  8. 8
    세척was washed with brine
  9. 9
    건조was dried (magnesium sulfate)
  10. 10
    기타was evaporated
  11. 11
    기타Purification by flash chromatography
  12. 12
    세척eluting with 2:1 hexanes/ether
  13. 13
    기타furthur purification of the mother liquor by flash chromatography
  14. 14
    세척eluting with 4:1 hexanes/ethyl acetate
  15. 15
    기타provided a white solid

실험 절차

n-Butyllithium (2.45M in hexanes, 5.7 mL, 13.96 mmol) was added dropwise over 5 min to a solution of trimethylsilylacetylene (1.97 mL, 13.96 mmol) dissolved in dry ether (30 mL) at -45° C. under an argon atmosphere. After 1.5 h, this solution was cannulated into a solution of dimethylaluminum chloride (1.0M in hexanes, 13.96 mL, 13.96 mmol). After 3.5 h at room temperature, the mixture was filtered through Celite® under an argon atmosphere. In a separate flask, diisobutylaluminum hydride (1.0M in toluene, 1.4 mL, 1.4 mmol) was added dropwise to a stirred mixture of nickel acetylacetonate (360 mg, 1.4 mmol) in dry ether (25 mL) at 0° C. under an argon atmosphere. After 10 min, the mixture was further cooled to -10° C. and the solution of aluminum acetylide was added via cannulation over 15 min. 3-(3-cyclopentyloxy-4-methoxyphenyl)cyclohex-2-en-1-one (2.0 g, 6.98 mmol, prepared as described in U.S. Pat. No. 5,362,915) dissolved in dry ether (70 mL) was added dropwise over 20 min. After 18 h at room temperature, the mixture was poured into a 100 mL saturated aqueous solution of potassium phosphate (monobasic) at 0° C., 100 mL of aqueous 3N HCl solution was added and the aqueous layer was extracted twice with ether. The combined extract was washed with brine, was dried (magnesium sulfate) and was evaporated. Purification by flash chromatography, eluting with 2:1 hexanes/ether followed by trituration from ether/hexanes, then furthur purification of the mother liquor by flash chromatography, eluting with 4:1 hexanes/ethyl acetate followed by trituration from ether/hexanes, provided a white solid. mp 102°-103° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723681uspto-grants-1998_03