Ammonia → 2-Amino-4-(3-chloropropyl)-6-trichloromethyl-1,3,5-triazine

HRID 745733Notes

Reaction equation

HRID 745733 reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][C:5]1[N:10]=[C:9]([C:11]([Cl:14])([Cl:13])[Cl:12])[N:8]=[C:7](C(Cl)(Cl)Cl)[N:6]=1.[NH3:19].O>O1CCCC1>[NH2:19][C:7]1[N:6]=[C:5]([CH2:4][CH2:3][CH2:2][Cl:1])[N:10]=[C:9]([C:11]([Cl:12])([Cl:13])[Cl:14])[N:8]=1

Participants

5

Reactant 3

HCID 222AmmoniaHCID 962WaterHCID 201996122-(gamma-Chloropropyl)4,6-bis-(trichloromethyl)-1,3,5-triazine

Product 1

HCID 201996142-Amino-4-(3-chloropropyl)-6-trichloromethyl-1,3,5-triazine

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

102.3 g of 2-(3-chloropropyl)-4,6-bis-(trichloromethyl)-1,3,5-triazine are dissolved in 100 ml of tetrahydrofuran, and to this solution are added, whilst it is being stirred at room temperature, 400 ml of concentrated aqueous ammonia solution. After 30 minutes are added 500 ml of water, and the reaction mixture is extracted twice with 100 ml of ether each time. The ether phases are dried over magnesium sulfate, filtered, and concentrated by evaporation to yield 68.3 g of the title product as light-brown oil.

Workup

  1. additionto this solution are added, whilst it
  2. extractionthe reaction mixture is extracted twice with 100 ml of ether each time
  3. dry with materialThe ether phases are dried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated by evaporation

Sources & evidence

ORD record
ord-2afc1f2c420b4679a0aff804f3b719fe
Source dataset
uspto-grants-1986_07
Patent number
US04600428

Reaction notes

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