Boron trifluoride etherate → 4-(5-Oxo-tetrahydro-furan-3-yl)-benzoic Acid Ethyl Ester

HRID 8200

反応式

HRID 8200 の反応式
ClC1C=CC=C(C(OO)=O)C=1.S([O-])([O-])(=O)=O.[Mg+2].B(F)(F)F.CCOCC.[CH2:27]([O:29][C:30](=[O:44])[C:31]1[CH:36]=[CH:35][C:34]([CH:37]2[CH2:41][CH:40]([O:42]C)[O:39][CH2:38]2)=[CH:33][CH:32]=1)[CH3:28]>ClCCl.CCOCC>[CH2:27]([O:29][C:30](=[O:44])[C:31]1[CH:32]=[CH:33][C:34]([CH:37]2[CH2:41][C:40](=[O:42])[O:39][CH2:38]2)=[CH:35][CH:36]=1)[CH3:28]

参加物

7

実験手順

To a solution of 75% 3-chloroperbenzoic acid (2.7 g, 11.76 mmol) in dichloromethane (35 mL) is added magnesium sulfate (2.0 g, 16.6 mmol) and the mixture stirred for 30 min. Solids are removed by filtration and the filtrate treated with borontrifluoride etherate (0.5 mL, 3.92 mmol) and 4-(5-methoxy-tetrahydro-furan-3-yl)-benzoic acid ethyl ester (2.45 g, 9.8 mmol) in dichloromethane (5 mL). The mixture is stirred at room temperature 18 h, diluted with ether (200 mL) and washed with a 10% solution of sodium thiosulfite (150 mL), a saturated solution of sodium bicarbonate (150 mL) and brine. The mixture is dried over magnesium sulfate, filtered and concentrated in vacuo. The residue is chromatographed on SiO2 (elute with 20% ethyl acetate/hexanes) to yield the title compound, 2.2 g (96%), as an off-white solid.

後処理

  1. customSolids are removed by filtration
  2. stirringThe mixture is stirred at room temperature 18 h
  3. washwashed with a 10% solution of sodium thiosulfite (150 mL)
  4. dry with materialThe mixture is dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue is chromatographed on SiO2 (elute with 20% ethyl acetate/hexanes)

出典と根拠

ORDレコード
ord-533050e5611d4df3b3683b95512ad06a
出典データセット
uspto-grants-2006_08
特許番号
US07087626B2

関連ノート

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