Potassium Fluoride → HCID 13282760, compound

HRID 2049939Notes

Reaction equation

HRID 2049939 reaction equation
Cl[C:2]1[S:3][C:4]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[C:5]([C:7]([F:10])([F:9])[F:8])[N:6]=1.[F-:16].[K+].[K]>O1CCOCCOCCOCCOCCOCC1>[F:16][C:2]1[S:3][C:4]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[C:5]([C:7]([F:10])([F:9])[F:8])[N:6]=1

Participants

5

Procedure

A mixture of 26 g (0.1 mole) of ethyl 2-chloro-4-trifluoromethyl-5-thiazolecarboxylate, 37 g (0.55 mole) of potassium fluoride, and 0.11 g of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-CROWN-6, Aldrich Chemical Company) was held at reflux for 23 hours. Since an analysis showed the reaction to be incomplete, another 45 g (0.77 mole) of potassium fluoride was added and the reaction mixture held at reflux for 64 hours. To said mixture, 0.15 g of 18-CROWN-6 and an additional 27 g (0.40 mole) of potassium was added and held at reflux for 22 hours. Due to poor cooling overnight some of the solvent had evaporated. The reaction mixture was cooled and 300 ml. of acetonitrile added. The acetonitrile was filtered and concentrated. The residue was Kugelrohr distilled to give 13.7 g of a material which was separated by spinning band column at 15 mm Hg to give 4.2 g of the desired product, nD24 =1.4348.

Workup

  1. temperatureat reflux for 23 hours
  2. customthe reaction
  3. temperatureat reflux for 64 hours
  4. temperatureat reflux for 22 hours
  5. temperatureDue to poor cooling overnight some of the solvent
  6. customhad evaporated
  7. temperatureThe reaction mixture was cooled
  8. additionof acetonitrile added
  9. filtrationThe acetonitrile was filtered
  10. concentrationconcentrated
  11. distillationdistilled

Sources & evidence

ORD record
ord-6803727148c3414e83a6c77da7803045
Source dataset
uspto-grants-1980_04
Patent number
US04199506

Reaction notes

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