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

HRID 537095Notes

Reaction equation

HRID 537095 reaction equation
[Br:1][C:2]1[N:6]([CH:7]([CH3:9])[CH3:8])[N:5]=[CH:4][C:3]=1[CH2:10]O.P(Br)(Br)[Br:13]>ClCCl>[Br:1][C:2]1[N:6]([CH:7]([CH3:9])[CH3:8])[N:5]=[CH:4][C:3]=1[CH2:10][Br:13]

Participants

4

Procedure

To a stirred solution of (5-bromo-1-isopropyl-1H-pyrazol-4-yl)methanol (10.0 g, 45.7 mmol) in dichloromethane (200 mL) was added PBr3 (6.5 mL, 68.5 mmol) at 0° C. After the addition was complete the mixture was allowed to warm to room temperature and stirred for 3 hours. The mixture was poured into ice-cold water (300 mL), shaken, separated, and then washed twice with ice-cold water (2×100 mL) and then brine (100 mL), dried over sodium sulfate, filtered and the solvent removed in vacuo to give 5-bromo-4-(bromomethyl)-1-isopropyl-1H-pyrazole (12.2 g, 95%). 1H NMR (300 MHz, CDCl3, δ): 7.58 (s, 1H), 4.64 (m, 1H), 4.35 (s, 2H), 1.43 (d, 6H).

Workup

  1. additionAfter the addition
  2. stirringshaken
  3. customseparated
  4. washwashed twice with ice-cold water (2×100 mL)
  5. dry with materialbrine (100 mL), dried over sodium sulfate
  6. filtrationfiltered
  7. customthe solvent removed in vacuo

Sources & evidence

ORD record
ord-fb8c8e85053041269630735d3d51fe51
Source dataset
uspto-grants-2014_10
Patent number
US08859773B2

Reaction notes

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