تفاعل #50641

ord-6e2bde15ea614367b321bcbbc2e47f11

معادلة التفاعل

NC(/C=C/c1ccc(Cl)c(C(F)(F)F)c1)=NO
(E)-4-chloro-3-trifluoromethylcinnamamide oxime
CCOC(OCC)OCC
triethyl orthoformate
FC(F)(F)c1cc(/C=C/c2ncon2)ccc1Cl
(E)-3-(4-chloro-3-trifluoromethyl-styryl)-1,2,4-oxadiazole
المردود 71.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONare added at room temperature
  2. 2
    درجة الحرارةat reflux temperature for 2 hours
  3. 3
    تركيزthe whole batch is then concentrated in vacuo
  4. 4
    غسيلwashed consecutively with 100 ml of 2N hydrochloric acid, saturated sodium carbonate solution and water
  5. 5
    تجفيفThe organic phase is dried over sodium sulphate
  6. 6
    workup.DISTILLATIONthe solvent is subsequently distilled off

الإجراء التجريبي

5.2 g (0.02 mol) of (E)-4-chloro-3-trifluoromethylcinnamamide oxime are initially introduced into 50 ml of triethyl orthoformate and 2 drops of boron trifluoride etherate are added at room temperature. The mixture is then stirred at reflux temperature for 2 hours and the whole batch is then concentrated in vacuo. The residue is then taken up in 100 ml of methylene chloride and washed consecutively with 100 ml of 2N hydrochloric acid, saturated sodium carbonate solution and water. The organic phase is dried over sodium sulphate and the solvent is subsequently distilled off. 3.9 g (71.0% of theory) of (E)-3-(4-chloro-3-trifluoromethyl-styryl)-1,2,4-oxadiazole are obtained.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05428049uspto-grants-1995_06