تفاعل #791931

ord-5c4a30a59ebc470a8bb4038ba1edcf5a

معادلة التفاعل

Cl
hydrochloric acid
CC(C)C(=O)CC(C(=O)c1ccccc1)c1ccc(F)cc1
compound
CC(C)C(=O)CC(C(=O)c1ccccc1)c1ccc(F)cc1
2-(4-Fluorophenyl)-5-methyl-1-phenyl-hexane-1,4-dione
NN1CCCCCC1
N-amino-hexahydroazepine
CN(C)C=O
dimethylformamide
CC(C)c1cc(-c2ccc(F)cc2)c(-c2ccccc2)n1C1CCCCCN1
3-(4-Fluorophenyl)-1-hexahydroazepinyl-5-isopropyl-2-phenyl-pyrrole

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture is cooled
  2. 2
    workup.ADDITIONdiluted
  3. 3
    استخلاصextracted three times
  4. 4
    تجفيفThe organic phase is dried over magnesium sulphate
  5. 5
    تركيزconcentrated in vacuo
  6. 6
    أخرىthe residue is chromatographed on a column (silica gel 70-230 mesh, using ethyl acetate/petroleum ether 1:9)

الإجراء التجريبي

1.7 ml of conc. hydrochloric acid are added to 5 g (16.7 mmol) of the compound from Example 2 and 5.7 g (50.1 mmol) of N-amino-hexahydroazepine in 100 ml of toluene AR and 80 ml of dimethylformamide and the mixture is boiled in a water separator for 24 hours. The mixture is cooled, diluted using 200 ml of ethyl acetate and extracted three times using 1N hydrochloric acid and twice using saturated sodium hydrogen carbonate solution. The organic phase is dried over magnesium sulphate and concentrated in vacuo, and the residue is chromatographed on a column (silica gel 70-230 mesh, using ethyl acetate/petroleum ether 1:9).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04988711uspto-grants-1991_01