반응 #7645

ord-806f557d0a9c4151b5de0201eb12a922

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도heated
  2. 2
    온도While heating
  3. 3
    온도at reflux
  4. 4
    온도The reaction mixture is heated
  5. 5
    온도at reflux until no more evolution of gas
  6. 6
    추출the organic phase extracted with ethyl acetate
  7. 7
    기타The dried organic phase is evaporated to dryness in vacuo
  8. 8
    workup.DISSOLUTIONdissolved in ethanol
  9. 9
    기타the solution directly used for the next reaction

실험 절차

1.6 g (8 mmol) 2-[(cyclopentylcarbonyl)amino]butanoic acid are suspended in 30 ml tetrahydrofurane and heated to reflux together with 1.91 g (24 mmol) pyridine and a bit of N,N-dimethylaminopyridine. While heating at reflux, 2.19 g (16 mmol) ethyl chloro(oxo)acetate are added dropwise. The reaction mixture is heated at reflux until no more evolution of gas can be observed. After cooling down to room temperature, the reaction mixture is added to ice water and the organic phase extracted with ethyl acetate. The dried organic phase is evaporated to dryness in vacuo, dissolved in ethanol and the solution directly used for the next reaction.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07087605B2uspto-grants-2006_08