반응 #1403
ord-d4e2b55500174bc5b7869b5b5174c913
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후처리
- 1workup.WAITAfter 3.5 h at room temperature
- 2여과the mixture was filtered through Celite® under an argon atmosphere
- 3workup.WAITAfter 10 min
- 4workup.ADDITIONwas added dropwise over 20 min
- 5workup.WAITAfter 18 h at room temperature
- 6추출the aqueous layer was extracted twice with ether
- 7추출The combined extract
- 8세척was washed with brine
- 9건조was dried (magnesium sulfate)
- 10기타was evaporated
- 11기타Purification by flash chromatography
- 12세척eluting with 2:1 hexanes/ether
- 13기타furthur purification of the mother liquor by flash chromatography
- 14세척eluting with 4:1 hexanes/ethyl acetate
- 15기타provided 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.