2,2,2-Trifluoroethanol → STK076603

HRID 1252645Notes

Reaction equation

HRID 1252645 reaction equation
[NH2:1][C:2]1[N:7]=[C:6](Cl)[N:5]=[C:4]([NH:9][CH3:10])[N:3]=1.[OH-].[K+].[F:13][C:14]([F:18])([F:17])[CH2:15][OH:16]>>[NH2:1][C:2]1[N:3]=[C:4]([NH:9][CH3:10])[N:5]=[C:6]([O:16][CH2:15][C:14]([F:18])([F:17])[F:13])[N:7]=1

Participants

4

Reactant 3

HCID 64092,2,2-TrifluoroethanolHCID 14797Potassium HydroxideHCID 2249702-Chloro-4-methylamino-6-amino-1,3,5-triazine-

Product 1

HCID 1375559STK076603

Procedure

2-Amino-4-chloro-6-methylamino-1,3,5-triazine (0.2 mole) was slurried in 80 ml of 2,2,2-trifluoroethanol at room temperature. Potassium hydroxide pellets (0.2 mole) were added portionwise and the mixture was stirred at room temperature overnight. The following day the reaction was heated at gentle reflux for 2 hours during which time the solids gradually dissolved. The solution was cooled and the solvent was removed under vacuum. The residue was washed with water and filtered to give 20.9 g shining off-white crystals of the product named above with the following characteristics: m.p. 204°-205° C. NMR (DMSO-d6): δ 2.75, d, (NHCH3); 4.8, q, (OCH2CF3); 6.5-7.3, m, (NH2 +NHCH3).

Workup

  1. temperatureThe following day the reaction was heated
  2. temperatureat gentle reflux for 2 hours during which time the solids
  3. dissolutiongradually dissolved
  4. temperatureThe solution was cooled
  5. customthe solvent was removed under vacuum
  6. washThe residue was washed with water
  7. filtrationfiltered
  8. customto give 20.9 g

Sources & evidence

ORD record
ord-d712683cafd14d8a9eacbbb8c7af22db
Source dataset
uspto-grants-1988_05
Patent number
US04744816

Reaction notes

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