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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630158Generated: November 1, 2026

Chlorosuccinimide → (4-chloro-1-methyl-1H-imidazol-5-yl)methanol

https://huagongshe.com/reaction/630158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant(1-methyl-1H-imidazol-5-yl)methanolHCID 2773450—
Solvent1,4-DioxaneHCID 31275—
Product(4-chloro-1-methyl-1H-imidazol-5-yl)methanolHCID 53991406—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315521B2
Source datasetuspto-grants-2016_04
ORD IDord-126edc9141e644c3b4b3c080dfcda190
Source noteuspto-grants-2016_04