Hydrochloric Acid → 1,3,5-Triazin-2-amine, 4-propoxy-6-(trifluoromethyl)-

HRID 654266

Reaktionsgleichung

Reaktionsgleichung von HRID 654266
[NH2:1][C:2]1[N:7]=[C:6](C(Cl)(Cl)Cl)[N:5]=[C:4]([C:12]([F:15])([F:14])[F:13])[N:3]=1.[CH2:16]([O-:19])[CH2:17][CH3:18].[Na+].Cl>C(O)CC>[NH2:1][C:2]1[N:7]=[C:6]([O:19][CH2:16][CH2:17][CH3:18])[N:5]=[C:4]([C:12]([F:15])([F:14])[F:13])[N:3]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
75 °C

Versuchsvorschrift

20.0 g (71 mmol) of 2-amino-4-trichloromethyl-6-trifluoromethyl-1,3,5-triazine were added at 22° C. to a solution of 0.58 g (7.1 mmol) of sodium propanolate in 40 ml of propanol. The resulting yellow mixture was then heated at 75° C. for 30 minutes, after which a further 0.58 g (7.1 mmol) of sodium propanolate in 10 ml of propanol was added and the mixture was heated at 75° C. for 10 minutes. The reaction mixture was cooled to 20° C. and then neutralized with 2 normal aqueous hydrochloric acid. After this, most of the solvent was removed under reduced pressure, and the residue was slowly diluted with 40 ml of water. The solid which formed was separated off, washed with 5 ml of water and dried at 40° C. under reduced pressure.

Aufarbeitung

  1. temperaturethe mixture was heated at 75° C. for 10 minutes
  2. temperatureThe reaction mixture was cooled to 20° C.
  3. customAfter this, most of the solvent was removed under reduced pressure
  4. additionthe residue was slowly diluted with 40 ml of water
  5. customThe solid which formed
  6. customwas separated off
  7. washwashed with 5 ml of water
  8. customdried at 40° C. under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-4b7baf73c2e7414297b71a36cdfe8b58
Quelldatensatz
uspto-grants-1992_07
Patentnummer
US05130428

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