反応 #7964

ord-6135e02ccc8a47dd9175ba392412cef1

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGThe resulting solution was stirred at 0° C. for 30 minutes
  2. 2
    workup.STIRRINGthen stirred at room temperature overnight
  3. 3
    抽出The aqueous phase was extracted with EtOAc (20 mL)
  4. 4
    洗浄the combined organics were washed with 5% NaHCO3 and brine
  5. 5
    乾燥dried over MgSO4
  6. 6
    ろ過filtered
  7. 7
    濃縮concentrated under vacuum to a yellow oil
  8. 8
    その他The crude product was purified by preparative layer chromatography on three 0.1×20×20 silica gel GF plates
  9. 9
    洗浄The UV visible band at Rf 0.44-0.56 was eluted with EtOAc
  10. 10
    その他the eluant evaporated under vacuum

実験手順

A solution of 9a-butyl-7-methoxymethoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (230 mg, 0.73 mmol) in anhydrous THF (3.8 mL) was cooled in an ice bath, stirred under a nitrogen atmosphere, and treated with freshly prepared 0.4M LDA in THF (2.2 mL, 0.88 mmol). The resulting solution was stirred at 0° C. for 30 minutes, then cooled to −78° C. (dry ice-acetone bath) and treated with allyl bromide (0.316 mL, 3.65 mmol). The reaction mixture was allowed to gradually warm to room temperature then stirred at room temperature overnight. The mixture was diluted with EtOAc (60 mL) and shaken with 1N HCl (35 mL). The aqueous phase was extracted with EtOAc (20 mL) and the combined organics were washed with 5% NaHCO3 and brine, dried over MgSO4, filtered, and concentrated under vacuum to a yellow oil. The crude product was purified by preparative layer chromatography on three 0.1×20×20 silica gel GF plates using 4:1 hexanes-EtOAc as developing solvent. The UV visible band at Rf 0.44-0.56 was eluted with EtOAc and the eluant evaporated under vacuum to afford (2SR,9aSR)-2-allyl-9a-butyl-7-methoxymethoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (193 mg) as an oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07087599B2uspto-grants-2006_08