반응 #1120645

ord-f43b8611b4f44220a86590f9de716ba0

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGwas stirred for 0.5 hour
  2. 2
    세척The organic layer was washed successively with a saturated sodium bicarbonate solution and brine
  3. 3
    건조dried over anhydrous sodium sulfate
  4. 4
    여과After filtration
  5. 5
    농축the filtrate was concentrated in vacuo

실험 절차

(3S,4S)-4-(1-Methylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone (200 g) was dissolved in ethyl acetate (3 liters), and a solution of chlorine in carbon tetrachloride (3.85%, 870 g) was added dropwise thereto at room temperature over a period of 15 minutes, followed by stirring for 1 hour. Water (1 liter) and then 10% aqueous sodium thiosulfate solution (50 ml) were poured into the reaction mixture, which was stirred for 0.5 hour and allowed to stand. The organic layer was washed successively with a saturated sodium bicarbonate solution and brine and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated in vacuo to give (3S,4S)-4-(1-chloromethylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone. m.p., 84°-85° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05310897uspto-grants-1994_05