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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589511Generated: October 26, 2026

Sodium hydride → isopropyl N-n-butoxymethyl-2-bromo-4-methyl-5-imidazolecarboxylate

https://huagongshe.com/reaction/1589511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-(Chloromethoxy)butaneHCID 11105357—
ReactantHCID 178432453HCID 178432453—
SolventTetrahydrofuranHCID 8028—
Productisopropyl N-n-butoxymethyl-2-bromo-4-methyl-5-imidazolecarboxylateHCID 1358903589%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 293 milligrams (mg) (1.22 mM) of sodium hydride in 30 ml of anhydrous tetrahydrofuran was added, in portions, 3 g (1.22 mM) of isopropyl 2-bromo-4-methyl-5-imidazolecarboxylate. The resulting suspension was cooled to 0° C. and 1.5 g (1.22 mM) of chloromethyl-n-butyl ether was added dropwise. The reaction mixture was stirred overnight at room temperature. The precipitated sodium chloride was removed by filtration and concentration of the filtrate in vacuo gave 3.6 g (89%) of the desired product, isopropyl N-n-butoxymethyl-2-bromo-4-methyl-5-imidazolecarboxylate as a golden oil (89% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04571257
Source datasetuspto-grants-1986_02
ORD IDord-d9a1e2668e6846cfb6bd42ea340d366e
Source noteuspto-grants-1986_02