Potassium Hydroxide → HCID 178506226, compound

HRID 1641709Notes

Reaction equation

HRID 1641709 reaction equation
[NH2:1][C:2](N)=[S:3].ClC1[CH:11]=[CH:10][C:9]([C:12]([F:15])([F:14])[F:13])=[CH:8]N=1.[OH-].[K+].[OH-].[Na+]>C(O)C.O.C(Cl)Cl>[F:13][C:12]([F:15])([F:14])[C:9]1[CH:10]=[CH:11][C:2]([SH:3])=[N:1][CH:8]=1

Participants

8

Procedure

Thiourea (684 mg, 8.80 mmol) was added to a solution of 2-chloro-5-(trifluoromethyl)pyridine (1.45 g, 8.00 mmol) in ethanol (4 ml), and the resulting mixture was heated to reflux for 2 hours. The reaction mixture was cooled to room temperature, subsequently a solution of potassium hydroxide (792 mg, 12.0 mmol) in water (4 ml) was added thereto, and the resulting mixture was heated to reflux for 2 hours. The reaction mixture was cooled again to room temperature, and 1 N sodium hydroxide and methylene chloride were added thereto. After the aqueous layer was separated, acetic acid added to the aqueous layer, which was then extracted with methylene chloride. The organic layer was dried over anhydrous sodium sulfate and filtered, and then the filtrate was concentrated under reduced pressure. The obtained residue was washed with a mixed solvent of to hexane and diethyl ether, and was collected by filtration to obtain the title compound (860 mg, 4.80 mmol, 60%) as a pale yellow solid.

Workup

  1. temperaturethe resulting mixture was heated
  2. temperatureto reflux for 2 hours
  3. temperaturethe resulting mixture was heated
  4. temperatureto reflux for 2 hours
  5. temperatureThe reaction mixture was cooled again to room temperature
  6. customAfter the aqueous layer was separated
  7. additionacetic acid added to the aqueous layer, which
  8. extractionwas then extracted with methylene chloride
  9. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  10. filtrationfiltered
  11. concentrationthe filtrate was concentrated under reduced pressure
  12. washThe obtained residue was washed with a mixed solvent of to hexane and diethyl ether
  13. filtrationwas collected by filtration

Sources & evidence

ORD record
ord-3e2ad9a308894e66ac417a9b186a53cd
Source dataset
uspto-grants-2012_02
Patent number
US08114886B2

Reaction notes

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