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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025552Generated: October 30, 2026

Sodium Methoxide → methyl 4-bromo-1-methyl-1H-imidazole-2-carboxylate

https://huagongshe.com/reaction/1025552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant1-(-4-bromo-1-methyl-1H-imidazol-2-yl)-2,2,2-trichloroethanoneHCID 70922263—
SolventMethanolHCID 887—
Productmethyl 4-bromo-1-methyl-1H-imidazole-2-carboxylateHCID 53302209337.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

To the solution of 1.18 g of 1-(-4-bromo-1-methyl-1H-imidazol-2-yl)-2,2,2-trichloroethanone in 10 mL of methanol was added 42 mg of sodium methoxide and the resulting mixture was stirred at 25° C. for 20 min. TLC showed completion of the reaction. The solution was evaporated, redissolved in 30 mL of DCM, washed with water (15 mL×2) and brine (15 mL). The solution was dried over anhydrous sodium sulfate and filtered. The residue was purified by silica gel column (DCM/MeOH=60/1) to give 4-bromo-1-methyl-1H-imidazole-2-carboxylic acid methyl ester (0.575 g, yield 68%). 1H NMR (300 MHz, CDCl3) δ 7.02 (s, 1H), 4.00 (s, 3H). 3.93 (s, 3H). LC-MS calcd for C6H7BrN2O2 (m/e) 217.97, obsd 219 and 221 [M+1]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729078B2
Source datasetuspto-grants-2014_05
ORD IDord-94ba507a7eb14213a5a2411c3308ce10
Source noteuspto-grants-2014_05