Potassium Carbonate → HCID 178509606, compound

HRID 25281

Reaction equation

HRID 25281 reaction equation
[S:1]([C:19]1[CH:24]=[C:23]([C:25]2[C:26]([C:30]([F:33])([F:32])[F:31])=[N:27][NH:28][CH:29]=2)[CH:22]=[CH:21][C:20]=1[C:34]#[N:35])[C:2]1C=C(C2C(C(F)(F)F)=NNC=2)C=CC=1C#N.C(S([O-])=O)O.[Na+].C(=O)([O-])[O-].[K+].[K+].[F:48][C:49]([F:53])([F:52])CI>CN(C)C=O.O>[F:48][C:49]([F:53])([F:52])[CH2:2][S:1][C:19]1[CH:24]=[C:23]([C:25]2[C:26]([C:30]([F:32])([F:33])[F:31])=[N:27][NH:28][CH:29]=2)[CH:22]=[CH:21][C:20]=1[C:34]#[N:35]

Participants

7

Procedure

2.7 g (5.0 mmol) of 1,1′-thiodi-[2-cyano-5-(3-trifluoromethylpyrazolyl)benzene], 3.0 g (19.5 mmol) of Rongalite, 3.0 g (21.7 mmol) of potassium carbonate and 6.1 g (29.0 mmol) of 2,2,2-trifluoroethyl iodide were stirred in 50 ml of N,N-dimethylformamide at room temperature for 3 hours. The resulting reaction mixture was poured into 300 ml of water and extracted with 50 ml of ethyl acetate twice. The ethyl acetate layer was washed with 50 ml of water twice and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 2.5 g of 2-(2,2,2-trifluoroethylthio)-4-(3-trifluoromethylpyrazolyl)benzonitrile (yield 71.4%) as a brown solid ((m.p. 65-67° C.).

Workup

  1. customThe resulting reaction mixture
  2. extractionextracted with 50 ml of ethyl acetate twice
  3. washThe ethyl acetate layer was washed with 50 ml of water twice
  4. dry with materialdried over anhydrous magnesium sulfate
  5. distillationthe ethyl acetate was distilled off under reduced pressure
  6. customPurification of the residue by silica gel column chromatography

Sources & evidence

ORD record
ord-c9347b97e34c483e90558cbfbf6f8014
Source dataset
uspto-grants-2005_02
Patent number
US06858639B2

Linked notes

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