تفاعل #80494

ord-48faca2029d943378334cf901ca61c11

معادلة التفاعل

CN(N=C(Cl)c1ccccc1Cl)S(=O)(=O)c1ccccc1
N-methyl-N-(benzenesulfonyl)-2-chlorobenzohydrazonoyl chloride
CCCCCCCCOc1cc(C#N)ccc1Cl
4-chloro-3-octyloxybenzonitrile
Clc1ccccc1Cl
o-dichlorobenzene
CCCCCCCCOc1cc(-c2nc(-c3ccccc3Cl)nn2C)ccc1Cl
desired compound
المردود 42.3%
CCCCCCCCOc1cc(-c2nc(-c3ccccc3Cl)nn2C)ccc1Cl
5-(4-chloro-3-octyloxyphenyl)-3-(2-chlorophenyl) 1-methyl-1H-1,2,4-triazole
المردود 42.3%

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-(benzenesulfonyl)-2-chlorobenzohydrazonoyl chloride (1.50 g), 4-chloro-3-octyloxybenzonitrile (1.30 g), anhydrous iron (III) chloride (0.80 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 0.80 g of desired compound.

المصدر

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