Cyanuric chloride → 2,4-Bis(2-methoxyethoxy)-1,3,5-triazine

HRID 2379505Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2379505
[CH3:1][O:2][CH2:3][CH2:4][OH:5].[N:6]1[C:13](Cl)=[N:12][C:10](Cl)=[N:9][C:7]=1Cl>C1(C)C=CC=CC=1.C(=O)([O-])[O-].[Na+].[Na+]>[CH3:1][O:2][CH2:3][CH2:4][O:5][C:7]1[N:9]=[CH:10][N:12]=[C:13]([O:5][CH2:4][CH2:3][O:2][CH3:1])[N:6]=1

Komponenten

5

Edukt 2

HCID 7954Cyanuric chlorideHCID 80192-Methoxyethanol

Produkt 1

HCID 1263052,4-Bis(2-methoxyethoxy)-1,3,5-triazineAusbeute 1.608,9 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1140TolueneLösungsmittelHCID 10340Sodium CarbonateLösungsmittel

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

In 100 ml of dry toluene containing 10 g of anhydrous sodium carbonate was dissolved 20 g of monomethoxypolyethylene glycol having an average molecular, weight of 4000 (Nippon Oil and Fats) and the solution was heated at 110° C. for 30 minutes. Then, 500 mg of cyanuric chloride was added and the mixture was heated at 110° C. for 24 hours. The reaction residue was filtered off, followed by addition of 300 ml of petroleum ether to cause precipitation. The precipitate was washed with several portions of petroleum ether to recover 10 g of 2,4-bis(O-methoxypolyethylene glycol)-6-chloro-s-triazine (yield 50%).

Aufarbeitung

  1. temperaturethe mixture was heated at 110° C. for 24 hours
  2. filtrationThe reaction residue was filtered off
  3. additionfollowed by addition of 300 ml of petroleum ether
  4. customprecipitation
  5. washThe precipitate was washed with several portions of petroleum ether

Quellen und Nachweise

ORD-Eintrag
ord-2771b1ab4af34a228c10e578736cca20
Quelldatensatz
uspto-grants-1994_11
Patentnummer
US05362853

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