تفاعل #80507
ord-77baf2e8159c40409244685c53cbc1a3
معادلة التفاعل
N-methyl-N-(benzenesulfonyl)-2,6-difluorobenzohydrazonoyl chloride
4-chloro-3-(5-trifluoromethylpyridine-2-yloxy)benzonitrile
o-dichlorobenzene
→
desired compound
المردود 24.6%
5-[4-chloro-3-(5-trifluoromethylpyridine-2-yloxy)phenyl]-3(2,6-difluorophenyl)-1-methyl-1H-1,2,4-triazole
المردود 24.6%
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
درجة الحرارة
140°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1درجة الحرارةAfter cooling
- 2غسيلwashed with dilute hydrochloric acid, dilute aqueous solution of sodium hydroxide and saline
- 3تجفيفThen, it is dried over anhydrous magnesium sulfate
- 4تركيزconcentrated under reduced pressure
- 5أخرىThe concentrate is purified by silica gel column chromatography
- 6workup.ADDITIONusing mixed solvent of hexaneethyl acetate as eluent
الإجراء التجريبي
A mixture of N-methyl-N-(benzenesulfonyl)-2,6-difluorobenzohydrazonoyl chloride (0.90 g), 4-chloro-3-(5-trifluoromethylpyridine-2-yloxy)benzonitrile (0.90 g), anhydrous iron (III) chloride (0.50 g) and o-dichlorobenzene (5 ml) is stirred at an oil bath temperature of 140° C. for 30 minutes. After cooling, it is dissolved in chloroform (100 ml) and washed with dilute hydrochloric acid, dilute aqueous solution of sodium hydroxide and saline. Then, it is dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The concentrate is purified by silica gel column chromatography using mixed solvent of hexaneethyl acetate as eluent to give 0.30 g of desired compound.