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Isopropanol → 1,2,3,3 a,8,8a-Hexahydro-alpha-oxo-1,3a,8-trimethyl-5-pyrrolo[2,3-b]indole acetic acid, isopropyl ester

HRID 1681637
ノート
印刷プレビュー

反応式

HRID 1681637 の反応式
[O:1]=[C:2]([C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[N:13]([CH3:17])[CH:12]1[N:18]([CH3:21])[CH2:19][CH2:20][C:11]21[CH3:22])[C:3]([O:5][CH2:6][CH3:7])=[O:4].[CH:23](O)(C)C>[O-]CC.[Ti+4].[O-]CC.[O-]CC.[O-]CC>[O:1]=[C:2]([C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[N:13]([CH3:17])[CH:12]1[N:18]([CH3:21])[CH2:19][CH2:20][C:11]21[CH3:22])[C:3]([O:5][CH:6]([CH3:23])[CH3:7])=[O:4]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 3776IsopropanolHCID 867464181,2,3,3a,8,8a-Hexahydro-alpha-oxo-1,3a,8-trimethyl-5-pyrrolo[2,3-b]indole acetic acid, ethyl ester

生成物 1

HCID 867464201,2,3,3 a,8,8a-Hexahydro-alpha-oxo-1,3a,8-trimethyl-5-pyrrolo[2,3-b]indole acetic acid, isopropyl ester

試薬・触媒・溶媒 1

HCID 76524Titanium tetraethoxide触媒

反応条件

温度
0 °C

実験手順

To a chilled (0° C.), stirred solution of 1,2,3,3a,8,8a-hexahydro-α-oxo-1,3a,8-trimethyl-5-pyrrolo[2,3-b]indole acetic acid, ethyl ester (0.68 g) in anhydrous isopropyl alcohol (10.2 ml) was added titanium (IV) ethoxide (0.17 ml) via syringe under a nitrogen atmosphere. The solution was warmed to room temperature and refluxed for 6.5 hours. The isopropyl alcohol was removed under reduced pressure and the residue dissolved in ethyl acetate (100 ml). The solution was washed twice with 50 ml portions of saturated aqueous NH4Cl solution, twice with 50 ml portions of saturated aqueous NaHCO3 solution and once with 50 ml of brine. The organic and aqueous phases were separated and the organic phase dried (Na2SO4), filtered, and concentrated to an oil. The crude mixture was purified using preparative HPLC (silica gel, 35% ethyl acetate in dichloromethane as the loading solvent and eluent). The appropriate fractions were combined and the solvents were removed under reduced pressure yielding 0.54 g of 1,2,3,3 a,8,8a-hexahydro-α-oxo-1,3a,8-trimethyl-5-pyrrolo[2,3-b]indole acetic acid, isopropyl ester, as an oil.

後処理

  1. temperatureThe solution was warmed to room temperature
  2. temperaturerefluxed for 6.5 hours
  3. customThe isopropyl alcohol was removed under reduced pressure
  4. dissolutionthe residue dissolved in ethyl acetate (100 ml)
  5. washThe solution was washed twice with 50 ml portions of saturated aqueous NH4Cl solution, twice with 50 ml portions of saturated aqueous NaHCO3 solution and once with 50 ml of brine
  6. customThe organic and aqueous phases were separated
  7. dry with materialthe organic phase dried (Na2SO4)
  8. filtrationfiltered
  9. concentrationconcentrated to an oil
  10. customThe crude mixture was purified
  11. customthe solvents were removed under reduced pressure

出典と根拠

ORDレコード
ord-a567bcffbf604219b391005e0906a370
出典データセット
uspto-grants-1992_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05173497

反応ノート

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