Water → 4-bromomethyl-3,5-dichloro-1-ethyl-1H-pyrazole

HRID 1292806Notes

Reaction equation

HRID 1292806 reaction equation
[Cl:1][C:2]1[C:6]([CH2:7]O)=[C:5]([Cl:9])[N:4]([CH2:10][CH3:11])[N:3]=1.P(Br)(Br)[Br:13].O>C(OCC)C>[Br:13][CH2:7][C:6]1[C:2]([Cl:1])=[N:3][N:4]([CH2:10][CH3:11])[C:5]=1[Cl:9]

Participants

5

Conditions

Temperature
-30 °C

Procedure

A solution of 0.82 g (4.2 mmoles) of (3,5-dichloro-1-ethyl-1H-pyrazol-4-yl)methanol dissolved in 50 ml of diethyl ether was cooled to −30° C. Thereto was added 1.3 g (4.8 mmoles) of phosphorus tribromide. The mixture was stirred at room temperature for 12 hours to give rise to a reaction. After confirmation of the completion of the reaction, the reaction mixture was poured into water, followed by extraction with ethyl acetate. The resulting organic layer was washed with water and an aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein, to obtain 0.9 g (yield: 81.8%) of 4-bromomethyl-3,5-dichloro-1-ethyl-1H-pyrazole as a yellow oily substance.

Workup

  1. customto give rise
  2. customto a reaction
  3. customAfter confirmation of the completion of the reaction
  4. extractionfollowed by extraction with ethyl acetate
  5. washThe resulting organic layer was washed with water
  6. dry with materialan aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate
  7. distillationThe resulting solution was subjected to vacuum distillation
  8. customto remove the solvent

Sources & evidence

ORD record
ord-b6c94891026f4a30870a10e45d8cdf62
Source dataset
uspto-grants-2007_07
Patent number
US07238689B2

Reaction notes

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