反应 #8282

ord-57fb327c6424452aa0687ad11e5803ae

反应方程式

CO.ClCCl
methanol dichloromethane
C=CCCC(=O)OCC
ethyl pent-4-enoate
C[N+]1([O-])CCOCC1
4-methylmorpholine N-oxide
C1CCOC1
tetrahydrofuran
CCOC(=O)CCC(O)CO
title compound
收率 96.0%
CCOC(=O)CCC(O)CO
4,5-Dihydroxy-pentanoic acid ethyl ester
收率 96.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩The mixture is concentrated in vacuo
  2. 2
    其他the residue chromatographed on SiO2 (2% methanol/ethyl acetate)

实验过程

A solution of ethyl pent-4-enoate (11.7 g, 91.3 mmol) in tetrahydrofuran (420 mL) and water (40 mL) is treated with osmium tetroxide (1.0 g, 4.2 mmol) and 4-methylmorpholine N-oxide (32.5 mL, 50% in water) at room temperature and stired for 3 h, at which time no more starting material is detectable by TLC (SiO2, 2% methanol/dichloromethane, Rf=0.40). The mixture is concentrated in vacuo and the residue chromatographed on SiO2 (2% methanol/ethyl acetate) to afford the title compound 14.37 g (96%) as a colorless oil.

来源

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