Phosphorus tribromide → 5-(bromomethyl)-4-chloro-1-methyl-1H-imidazole

HRID 577117Notes

Reaction equation

HRID 577117 reaction equation
[Cl:1][C:2]1[N:3]=[CH:4][N:5]([CH3:9])[C:6]=1[CH2:7]O.[Br:10]P(Br)Br>C(Cl)(Cl)Cl>[Br:10][CH2:7][C:6]1[N:5]([CH3:9])[CH:4]=[N:3][C:2]=1[Cl:1]

Participants

4

Procedure

To the solution of (1-methyl-1H-imidazol-5-yl)methanol (1.14 g, 10 mmol) in dioxane (50 mL), in a 250 mL round bottom flask, was added 1-chloropyrrolidine-2,5-dione (1.38 g, 10 mmol). The resulting mixture was stirred at room temperature overnight. Dioxane was removed under vacuum to provide (4-chloro-1-methyl-1H-imidazol-5-yl)methanol. The crude (4-chloro-1-methyl-1H-imidazol-5-yl)methanol was dissolved in 40 mL of chloroform, followed by addition of tribromophosphane (1.9 mL, 20 mmol). The resulting mixture was stirred at room temperature overnight. The solvent was evaporated to provide 5-(bromomethyl)-4-chloro-1-methyl-1H-imidazole.

Workup

  1. customThe solvent was evaporated

Sources & evidence

ORD record
ord-0cf4967bb02b4bc791e66aa4063126da
Source dataset
uspto-grants-2015_05
Patent number
US09040538B2

Reaction notes

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