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
反応物 4
生成物 1
試薬・触媒・溶媒 2
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
- customSolids are removed by filtration
- stirringThe mixture is stirred at room temperature 18 h
- washwashed with a 10% solution of sodium thiosulfite (150 mL)
- dry with materialThe mixture is dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- 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
読み込み中…