3-Dimethylamino-3'-trifluoromethylacrylophenone → HCID 11198195, compound

HRID 1447910Notes

Reaction equation

HRID 1447910 reaction equation
[NH2:1][C:2]1[NH:6][N:5]=[C:4]([CH2:7][C:8]#[N:9])[C:3]=1[C:10]#[N:11].CN(C)[CH:14]=[CH:15][C:16]([C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([C:24]([F:27])([F:26])[F:25])[CH:19]=1)=O>C(O)(=O)C>[C:10]([C:3]1[C:4]([CH2:7][C:8]#[N:9])=[N:5][N:6]2[C:16]([C:18]3[CH:19]=[C:20]([C:24]([F:25])([F:26])[F:27])[CH:21]=[CH:22][CH:23]=3)=[CH:15][CH:14]=[N:1][C:2]=12)#[N:11]

Participants

4

Procedure

A mixture of 2.94 g. of 5-amino-4-cyano-3-cyanomethyl pyrazole and 4.86 g. of 3-dimethylamino-3'-trifluoromethylacrylophenone in 25 ml. of glacial acetic acid is refluxed for 16 hours. The reaction mixture is evaporated to dryness and then extracted with methylene chloride. This solution is washed with a saturated sodium bicarbonate solution and dried with sodium sulfate. After passage of this solution through a short column of hydrous magnesium silicate, the effluent from this column is refluxed with gradual addition of hexane until the product crystallizes. Filtration gives crystals, m.p. 180°-181° C.

Workup

  1. additionA mixture of 2.94 g
  2. customThe reaction mixture is evaporated to dryness
  3. extractionextracted with methylene chloride
  4. washThis solution is washed with a saturated sodium bicarbonate solution
  5. dry with materialdried with sodium sulfate
  6. temperatureAfter passage of this solution through a short column of hydrous magnesium silicate, the effluent from this column is refluxed with gradual addition of hexane until the product
  7. customcrystallizes
  8. filtrationFiltration
  9. customgives crystals, m.p. 180°-181° C.

Sources & evidence

ORD record
ord-3013057b2d0a48a2becf3b206a8e1654
Source dataset
uspto-grants-1979_12
Patent number
US04178449

Reaction notes

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