反应 #8296

ord-533050e5611d4df3b3683b95512ad06a

反应方程式

CCOCC.FB(F)F
borontrifluoride etherate
CCOC(=O)c1ccc(C2COC(OC)C2)cc1
4-(5-methoxy-tetrahydro-furan-3-yl)-benzoic acid ethyl ester
O=C(OO)c1cccc(Cl)c1
3-chloroperbenzoic acid
O=S(=O)([O-])[O-].[Mg+2]
magnesium sulfate
CCOC(=O)c1ccc(C2COC(=O)C2)cc1
title compound
CCOC(=O)c1ccc(C2COC(=O)C2)cc1
4-(5-Oxo-tetrahydro-furan-3-yl)-benzoic acid ethyl ester

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Solids are removed by filtration
  2. 2
    workup.STIRRINGThe mixture is stirred at room temperature 18 h
  3. 3
    洗涤washed with a 10% solution of sodium thiosulfite (150 mL)
  4. 4
    干燥The mixture is dried over magnesium sulfate
  5. 5
    过滤filtered
  6. 6
    浓缩concentrated in vacuo
  7. 7
    其他The residue is chromatographed on SiO2 (elute with 20% ethyl acetate/hexanes)

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07087626B2uspto-grants-2006_08