Phosphorus tribromide → 5-Bromo-4-(bromomethyl)-1-(1,1-dimethylethyl)-1H-pyrazole

HRID 537088Notes

Reaction equation

HRID 537088 reaction equation
[Br:1][C:2]1[N:6]([C:7]([CH3:10])([CH3:9])[CH3:8])[N:5]=[CH:4][C:3]=1[CH2:11]O.P(Br)(Br)[Br:14]>ClCCl>[Br:1][C:2]1[N:6]([C:7]([CH3:10])([CH3:9])[CH3:8])[N:5]=[CH:4][C:3]=1[CH2:11][Br:14]

Participants

4

Conditions

Temperature
0 °C

Procedure

A solution of (5-bromo-1-tert-butyl-1H-pyrazol-4-yl)methanol (460 mg, 1.97 mmol) in dichloromethane (25 mL) was cooled to 0° C. and then treated with phosphorus(III)bromide (0.37 mL, 3.46 mmol), dropwise, over 5 minutes. The mixture was stirred 30 minutes at 0° C. and then 1 hour at room temp. The mixture was quenched slowly with water (50 mL), stirred 30 minutes, and then extracted with ethyl acetate (2×50 mL). The organic phase was washed with saturated aqueous sodium bicarbonate (50 mL), dried over sodium sulfate, filtered and concentrated to yield 362 mg of 5-bromo-4-(bromomethyl)-1-tert-butyl-1H-pyrazole as a clear oil. 1H NMR (400 MHz, CDCl3, δ): 7.54 (s, 1H), 4.39 (s, 2H), 1.74 (s, 9H).

Workup

  1. custom1 hour
  2. customat room temp
  3. customThe mixture was quenched slowly with water (50 mL)
  4. stirringstirred 30 minutes
  5. extractionextracted with ethyl acetate (2×50 mL)
  6. washThe organic phase was washed with saturated aqueous sodium bicarbonate (50 mL)
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-6a29591c17de4bfdabd514a3b38eff7a
Source dataset
uspto-grants-2014_10
Patent number
US08859773B2

Reaction notes

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