تفاعل #80500

ord-4141c9a6c7d8420fb4ce607437f93ee4

معادلة التفاعل

Cc1ccc(S(=O)(=O)N(C)N=C(Cl)c2c(F)cccc2Cl)cc1
N-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chloride
N#Cc1ccc(Oc2ccccc2)cc1Cl
2-chloro-4-phenoxybenzonitrile
Clc1ccccc1Cl
o-dichlorobenzene
Cn1nc(-c2c(F)cccc2Cl)nc1-c1ccc(Oc2ccccc2)cc1Cl
desired compound
المردود 4.1%
Cn1nc(-c2c(F)cccc2Cl)nc1-c1ccc(Oc2ccccc2)cc1Cl
3-(2-chloro-6-fluorophenyl)-5-(2-chloro-4-phenoxyphenyl) 1-methyl-1H-1,2,4-triazole
المردود 4.1%

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 hexane-ethyl acetate as eluent

الإجراء التجريبي

A mixture of N-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chloride (3.30 g), 2-chloro-4-phenoxybenzonitrile (2.30 g), anhydrous iron (III) chloride (1.60 g) and o-dichlorobenzene (10 ml) is stirred at an oil bath temperature of 140° C. for 1 hour. After cooling, the reaction mixture is dissolved in chloroform (100 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 hexane-ethyl acetate as eluent to give 0.15 g of desired compound (melting point: 135.0°-140.0° C.).

المصدر

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