Cyanuric chloride → 2,4-Dichloro-6-morpholino-1,3,5-triazine

HRID 1513410Notes

Reaction equation

HRID 1513410 reaction equation
[N:1]1[C:8]([Cl:9])=[N:7][C:5](Cl)=[N:4][C:2]=1[Cl:3].[NH:10]1[CH2:15][CH2:14][O:13][CH2:12][CH2:11]1.CCN(CC)CC>C(Cl)Cl>[Cl:9][C:8]1[N:1]=[C:2]([Cl:3])[N:4]=[C:5]([N:10]2[CH2:15][CH2:14][O:13][CH2:12][CH2:11]2)[N:7]=1

Participants

5

Reactant 3

HCID 7954Cyanuric chlorideHCID 8083MorpholineHCID 8471Triethylamine

Product 1

HCID 810762,4-Dichloro-6-morpholino-1,3,5-triazineYield 95.4%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Conditions

Temperature
-78 °C

Procedure

To a solution of cyanuric chloride (2.5 g, 13.5 mmol) in CH2Cl2 (150 mL) was added dropwise morpholine (1.14 g, 13.5 mmol) at −78° C., followed by addition of Et3N (3.0 mL, 21.5 mmol). The resulting reaction mixture was stirred at −78° C. for 20 min, and then diluted with CH2Cl2. The organic phase was washed with water and brine, and dried over MgSO4. The solvent was removed in vacuum to give the title compound as white crystalline solid (3.027 g, 95% yield). MS (ESI) m/z 235.1.

Workup

  1. customThe resulting reaction mixture
  2. washThe organic phase was washed with water and brine
  3. dry with materialdried over MgSO4
  4. customThe solvent was removed in vacuum

Sources & evidence

ORD record
ord-b73897e8ac3243b3a33733089c8a2a20
Source dataset
uspto-grants-2012_07
Patent number
US08217036B2

Reaction notes

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