Potassium Hydroxide → 3-(3-chloro-1H-pyrazol-1-yl)pyridine

HRID 1482404Notes

Reaction equation

HRID 1482404 reaction equation
[Cl:1][C:2]1[CH2:6][CH2:5][N:4]([C:7]2[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=2)[N:3]=1.[OH-].[K+]>O.C(#N)C.[Fe-3](C#N)(C#N)(C#N)(C#N)(C#N)C#N.[K+].[K+].[K+]>[Cl:1][C:2]1[CH:6]=[CH:5][N:4]([C:7]2[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=2)[N:3]=1

Participants

6

Conditions

Temperature
60 °C

Procedure

Crude 3-(3-chloro-4,5-dihydro-1H-pyrazol-1-yl)pyridine (54.1 g, 232 mmol, 77.8% purity) was introduced into a 3 L three-neck round bottom flask. Water (530 mL) was then added. The mixture was heated to 60° C. and a potassium hydroxide solution (165 g, 2940 mmol) in water (500 mL) was added. The dark brown mixture was heated to 90° C. A potassium ferricyanide solution (253 g, 768 mmol) in water (700 mL) was added slowly over 30 minutes leading to brown-red mixture. The mixture was stirred at 90° C. for another 1.5 hours. The reaction mixture was cooled to below 45° C. and filtered. The filter cake was washed with water (300 mL) affording crude product as a brown solid. The crude product was then dissolved in acetonitrile (400 mL) and filtered. The organic filtrate was dried and concentrated to afford the title product as a brown solid (28.8 g, 69%, 94% purity).

Workup

  1. temperatureThe dark brown mixture was heated to 90° C
  2. temperatureThe reaction mixture was cooled to below 45° C.
  3. filtrationfiltered
  4. washThe filter cake was washed with water (300 mL)
  5. customaffording crude product as a brown solid
  6. filtrationfiltered
  7. customThe organic filtrate was dried
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-0b39f45b79e14dbea0b4ef356a9ff862
Source dataset
uspto-grants-2016_08
Patent number
US09414594B2

Reaction notes

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