반응 #747152

ord-071013e725fc411eb1470c33e71805d9

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도under reflux
  2. 2
    농축The reaction mixture is concentrated under reduced pressure
  3. 3
    세척the mixture is washed with 1 N aqueous sodium hydroxide solution
  4. 4
    추출The aqueous phase is extracted repeatedly with ethyl acetate
  5. 5
    건조the combined organic phase is dried over sodium sulphate
  6. 6
    농축The organic phase is concentrated under reduced pressure
  7. 7
    기타the residue is purified by recrystallisation from ethyl acetate/cyclohexane

실험 절차

On a water separator, 550 mg (4.97 mmol) of 2-fluoroethylamine hydrochloride, 547 mg (5.47 mmol) of tetronic acid, 408 mg (4.97 mmol) of sodium acetate and 9 mg (0.05 mmol) of 4-toluenesulphonic acid in 50 ml of toluene are heated for 5 hours under reflux. The reaction mixture is concentrated under reduced pressure, the residue is taken up in ethyl acetate and the mixture is washed with 1 N aqueous sodium hydroxide solution. The aqueous phase is extracted repeatedly with ethyl acetate and the combined organic phase is dried over sodium sulphate. The organic phase is concentrated under reduced pressure and the residue is purified by recrystallisation from ethyl acetate/cyclohexane, giving 300 mg (42% of theory) of 4-[(2-fluoroethyl)amino]furan-2(5H)-one.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08084452B2uspto-grants-2011_12