反応 #55857

ord-81fabdb1a40044d5a7054b95e48411d2

反応方程式

C#Cc1cccc(O)c1
m-ethynylphenol
[Na+].[OH-]
NaOH
Clc1nc(Cl)nc(Cl)n1
cyanuric chloride
C#Cc1cccc(Oc2nc(Cl)nc(Oc3cccc(C#C)c3)n2)c1
bis-(m-ethynylphenoxy)-chloro-1,3,5-triazine
収率 95.8%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGAfter stirring for one hour at this temperature
  2. 2
    ろ過the resulting mixture is filtered
  3. 3
    その他to remove a white solid which
  4. 4
    洗浄is washed with water
  5. 5
    その他dried in vacuum overnight at 35° C
  6. 6
    温度increases to 127°-128° C. upon one recrystallization from chloroform/heptane

実験手順

The bis-(m-ethynylphenoxy)-chloro-1,3,5-triazine is prepared by first adding m-ethynylphenol (11.4 g, 0.097 mole) in 20 ml of a 5 N NaOH dropwise to a stirred solution of cyanuric chloride (9.22 g, 0.05 mole) in 50 ml of acetone with stirring at 15°-18° C. After stirring for one hour at this temperature, the resulting mixture is filtered to remove a white solid which is washed with water and dried in vacuum overnight at 35° C. The yield of the product is 16.14 g (yield of 95.8%). The product has a melting point of 121°-125° C. which increases to 127°-128° C. upon one recrystallization from chloroform/heptane. This product is analyzed by NMR and determined to be bis-(m-ethynylphenoxy)-chloro-1,3,5-triazine represented by the formula:

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04221895uspto-grants-1980_09