تفاعل #80493

ord-326a3fd6904b4d52a3ec1adb82efa881

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
CCCCCOc1cc(C#N)ccc1Cl
4-chloro-3-pentyloxybenzonitrile
Clc1ccccc1Cl
o-dichlorobenzene
CCCCCOc1cc(-c2nc(-c3c(F)cccc3Cl)nn2C)ccc1Cl
desired compound
المردود 41.8%
CCCCCOc1cc(-c2nc(-c3c(F)cccc3Cl)nn2C)ccc1Cl
3-(2-chloro-6-fluorophenyl)-5-(4-chloro-3-pentyloxyphenyl) 1-methyl-1H-1,2,4triazole
المردود 41.8%

المذيبات

ظروف التفاعل

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

المعالجة

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

الإجراء التجريبي

A mixture of N-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chloride (1.10 g), 4-chloro-3-pentyloxybenzonitrile (0.70 g), anhydrous iron (III) chloride (0.60 g) and o-dichlorobenzene (5 ml) is stirred at an oil bath temperature of 140° C. for 30 minutes. After cooling, the reaction mixture is dissolved in chloroform (100 ml), washed with dilute hydrochloric 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 0.50 g of desired compound.

المصدر

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