반응 #96242

ord-0274a580b3a24b3f8edf1ec0ecff52b0

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도under cooling in an ice-bath
  2. 2
    기타after removal of the solvent under vacuo, 7 ml of diethyl ether
  3. 3
    workup.ADDITIONwas added
  4. 4
    기타the clear liquid layer was separated
  5. 5
    기타evaporated to dryness under vacuo
  6. 6
    workup.WAITThe residue was kept at a pressure of 0.5 mm of mercury for half an hour

실험 절차

123 mg of tri-n-propylchlorosilane were added to a suspension of 312 mg of 7-benzamido-2-bromo-3-bromomethyl-3-cephem-4-carboxylic acid-1-oxide (prepared by the process of Step D of Example 1) in 25 ml of 1,2-dichloroethane under a nitrogen atmosphere and then a solution of 64 mg of triethyl-amine in 4 ml of 1,2-dichloroethane was dropwise added over 15 minutes under cooling in an ice-bath. The clear, slightly yellow colored solution was stirred for two hours at room temperature and after removal of the solvent under vacuo, 7 ml of diethyl ether was added. The obtained suspension was centrifuged and the clear liquid layer was separated and evaporated to dryness under vacuo. The residue was kept at a pressure of 0.5 mm of mercury for half an hour to obtain 210 mg of tri-n-propylsilyl 7-benzamido-2-bromo-3-bromomethyl-3-cephem-4-carboxylate-1-oxide having the following characteristics:

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04347358uspto-grants-1982_08