تفاعل #80496

ord-81c35234dda44d53a6bd8b273a56cc05

معادلة التفاعل

CN(N=C(Cl)c1c(F)cccc1Cl)S(=O)(=O)c1ccccc1
N-methyl-N-(benzenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chloride
N#Cc1ccc(Cc2ccc(Cl)c(Cl)c2)c(Cl)c1
3-chloro-4-(3,4-dichlorobenzyl)benzonitrile
Cn1nc(-c2c(F)cccc2Cl)nc1-c1ccc(Cc2ccc(Cl)c(Cl)c2)c(Cl)c1
desired compound
المردود 48.0%
Cn1nc(-c2c(F)cccc2Cl)nc1-c1ccc(Cc2ccc(Cl)c(Cl)c2)c(Cl)c1
5-[3-chloro-4-(3,4-dichlorobenzyl)phenyl]3-(2-chloro-6-fluorophenyl)-1-methyl-1H-1,2,4-triazole
المردود 48.0%

المذيبات

ظروف التفاعل

درجة الحرارة
140°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةAfter cooling
  2. 2
    غسيلwashed
  3. 3
    workup.ADDITIONwith dilute hydrochrolic acid, dilute aqueous solution of sodium hydroxide and saline in this order
  4. 4
    تجفيفdried over anhydrous magnesium sulfate
  5. 5
    تركيزconcentrated under reduced pressure
  6. 6
    أخرىThe concentrate is purified by silica gel column chromatography
  7. 7
    workup.ADDITIONusing mixed solvent of hexaneethyl acetate as eluent

الإجراء التجريبي

A mixture of N-methyl-N-(benzenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chloride (1.00 g), 3-chloro-4-(3,4-dichlorobenzyl)benzonitrile (0.93 g), anhydrous iron (III) chloride (0.50 g) and o-dichtorobenzene (5 ml) is stirred at an oil bath temperature of 140° C. for 1 hour. After cooling, the reaction mixture is dissolved in chloroform (300 ml), washed with dilute hydrochrolic acid, dilute aqueous solution of sodium hydroxide and saline in this order, 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 0.64 g of desired compound (melting point: 179.0°-185.0° C.).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05616594uspto-grants-1997_04