반응 #7967

ord-6d0e5e3c98d34755babed58fc6c14987

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The solvent was evaporated under vacuum
  2. 2
    세척washed with 0.2N HCl (30 mL), 5% NaHCO3, and brine
  3. 3
    건조dried over MgSO4
  4. 4
    여과filtered
  5. 5
    농축concentrated under vacuum to a gum (24 mg)
  6. 6
    기타This material was purified by PLC on a 0.1×20×20 cm silica gel GF plate

실험 절차

A solution of (2RS,9aSR)-9a-butyl-7-hydroxy-4-methyl-2-(2-oxo-ethyl)-1,2,9,9a-tetrahydro-3H-fluoren-3-one (17 mg, 0.05 mmol) in 2-propanol (2 mL) was treated with NaBH4 (1.9 mg, 0.05 mmol) and the mixture was stirred at room temperature for 40 minutes. The solvent was evaporated under vacuum. The residue was taken up in EtOAc (60 mL), washed with 0.2N HCl (30 mL), 5% NaHCO3, and brine, dried over MgSO4, filtered, and concentrated under vacuum to a gum (24 mg). This material was purified by PLC on a 0.1×20×20 cm silica gel GF plate using 2:1 hexanes-EtOAc as developing solvent. The UV visible band at Rf 0.06-0.11 afforded (2RS,9aSR)-9a-butyl-7-hydroxy-2-(2-hydroxyethyl)-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one as an oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07087599B2uspto-grants-2006_08