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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362458Generated: November 3, 2026

Imidazole → 5-(1H-Imidazol-1-yl)-2-methoxybenzoic acid, methyl ester

https://huagongshe.com/reaction/362458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium BromideHCID 253877—
ReactantMethyl 5-bromo-2-methoxybenzoateHCID 13297188—
SolventDimethylformamideHCID 6228—
Product5-(1H-Imidazol-1-yl)-2-methoxybenzoic acid, methyl esterHCID 16105649—

Reaction Steps

5-Bromo-2-methoxybenzoic acid, methyl ester (5 g, 20.4 mmol), imidazole (1.4 g, 20.6 mmol), and potassium carbonate (2.9 g, 20.7 mmol) were heated to 145° C. in DMF under N2 as cuprous iodide (1.5 g, 7.9 mmol) was added in portions. The reaction was stirred at this temperature for 18 h, allowed to cool, and filtered through a celite plug. The filtered salts were washed extensively with methanol, the filtrate concentrated in vacuo, and the residue taken up in ethyl acetate, washed with water, brine, and dried. Chromatography on SiO2, elution with methanol/ethyl acetate/hexanes (1:1:3) gave 3 g (63%); IR(KBr, ν=cm-1) 3430, 1726, 1512, 1232, 1068; 1H NMR (300 MHz, DMSO-d6) δ3.80 (3H, s), 3.85 (3H, s), 7.07 (1H, s), 7.27 (1H, d, J=8.8 Hz), 7.69 (1H, s), 7.76-7.82 (2H, m) 8.18 (1H, s); MS(DCl)m/z: 233 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869509
Source datasetuspto-grants-1999_02
ORD IDord-604e46f515b649ea8dbbb123940f5be2
Source noteuspto-grants-1999_02