تفاعل #1442520

ord-11c92f9a8fdb4125a2508328dac426ad

معادلة التفاعل

O=C1OC(=O)C(c2ccc(Cl)cc2)=C1Cl
3-chloro-4-(4-chlorophenyl)furan-2,5-dione
CN(N)c1ccccc1
N-methyl-N-phenylhydrazine
CN(c1ccccc1)N1C(=O)C(Cl)=C(c2ccc(Cl)cc2)C1=O
3-Chloro-4-(4-chlorophenyl)-1-(N-methyl-N-phenylamino)pyrrol-2,5-dione

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe mixture was then concentrated under reduced pressure
  2. 2
    غسيلwashed three times with in each case 150 ml of water
  3. 3
    تجفيفdried over sodium sulfate
  4. 4
    تركيزconcentrated under reduced pressure

الإجراء التجريبي

3.65 g (15 mmol) of 3-chloro-4-(4-chlorophenyl)furan-2,5-dione were initially charged in 75 ml of chloroform and, at room temperature, admixed dropwise with stirring with 1.83 g (15 mmol) of N-methyl-N-phenylhydrazine dissolved in 15 ml of chloroform, and the mixture was stirred at room temperature overnight. The mixture was then concentrated under reduced pressure and the residue was taken up in 200 ml of methylene chloride, washed three times with in each case 150 ml of water, dried over sodium sulfate and concentrated under reduced pressure. Yield: 4.6 g of a crystalline solid, m.p. 155-157° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06586369B1uspto-grants-2003_07