반응 #348448

ord-87fa02c272864a2db4cf164a497aaddb

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe solution was further stirred for 5 hours
  2. 2
    workup.WAITto stand overnight at room temperature
  3. 3
    기타Precipitates
  4. 4
    여과were filtered off
  5. 5
    workup.ADDITIONthe filtrate was poured into ice-water
  6. 6
    추출extracted with ethyl acetate
  7. 7
    세척The extract was washed with water
  8. 8
    기타dried
  9. 9
    기타The residue obtained
  10. 10
    workup.DISTILLATIONby distilling off the solvent under reduced pressure
  11. 11
    기타was crystallized by a small amount of ether

실험 절차

2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylate (0.54 g) was dissolved in absolute dimethylsulfoxide (5 ml). To this solution was added silver fluoroborate (0.20 g) and then the mixture was stirred under shielding from light for 3 hours at room temperature. To the solution was added a solution of triethylamine (0.1 g) in dimethylsulfoxide (0.5 ml) and the solution was further stirred for 5 hours and then allowed to stand overnight at room temperature. Precipitates were filtered off and the filtrate was poured into ice-water and then extracted with ethyl acetate. The extract was washed with water and dried. The residue obtained by distilling off the solvent under reduced pressure was crystallized by a small amount of ether to give colorless crystals of 2,2,2-trichloroethyl 3-hydroxy-3-methyl-7-(2-phenylacetamido)cepham-4-carboxylate (280 mg) (58%). This substance was recrystallized from a mixed solvent of benzene-n-hexane to give colorless needles melting at 169° to 171° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04164497uspto-grants-1979_08