Diethyl Ether → HCID 22618414, compound

HRID 1078438Notes

Reaction equation

HRID 1078438 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[C:4]([Cl:12])[C:3]=1[N:13]1[CH:17]=[C:16]([S:18][C:19]([F:22])([F:21])[F:20])[C:15]([CH:23]([OH:25])[CH3:24])=[N:14]1.[Cr](Cl)([O-])(=O)=O.[NH+]1C=CC=CC=1.CCOCC>ClCCl>[C:23]([C:15]1[C:16]([S:18][C:19]([F:20])([F:21])[F:22])=[CH:17][N:13]([C:3]2[C:2]([Cl:1])=[CH:7][C:6]([C:8]([F:9])([F:11])[F:10])=[CH:5][C:4]=2[Cl:12])[N:14]=1)(=[O:25])[CH3:24]

Participants

5

Reactant 3

HCID 3283Diethyl EtherHCID 22618617HCID 22618617, compoundHCID 178418287HCID 178418287, compound

Product 1

HCID 22618414HCID 22618414, compoundYield 36.5%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(1-hydroxyethyl)-4-trifluoromethylthiopyrazole (1.1 g) in dichloromethane (40 ml) was added pyridinium chlorochromate (0.62 g), and the mixture stirred at room temperature overnight. Ether (50 ml) was added and the mixture filtered on diatomaceous earth. Evaporation of the filtrate in vacuo gave a brown solid, which was triturated with hexane and filtered. The filtrate was evaporated in vacuo to give a yellow solid, which recrystallised from cyclohexane to give 3-acetyl-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylthiopyrazole (0.4 g) in the form of a yellow solid, m.p. 89°-91° C.

Workup

  1. filtrationthe mixture filtered on diatomaceous earth
  2. customEvaporation of the filtrate in vacuo
  3. customgave a brown solid, which
  4. customwas triturated with hexane
  5. filtrationfiltered
  6. customThe filtrate was evaporated in vacuo
  7. customto give a yellow solid, which
  8. customrecrystallised from cyclohexane

Sources & evidence

ORD record
ord-0a02e75ba84f453aa99676f45096080e
Source dataset
uspto-grants-1996_08
Patent number
US05547974

Reaction notes

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