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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356595Generated: October 31, 2026

Tetrahydrofuran → 1-(3-Ethoxyphenyl)-2-(4-fluorophenyl)-1H-imidazole-4-carboxylic acid

https://huagongshe.com/reaction/2356595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant3-EthoxyanilineHCID 12120—
Reactant4-FluorobenzonitrileHCID 14517—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 178466609HCID 178466609—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
Product1-(3-Ethoxyphenyl)-2-(4-fluorophenyl)-1H-imidazole-4-carboxylic acidHCID 59384153—

Reaction Steps

N-(3-Ethoxyphenyl)-4-fluorobenzenecarboximidamide To a solution of 2.2 ml (4.4 mmol) of 2.0 M (in tetrahydrofuran) sodium bis(trimethylsilyl)amide in 5.0 mL of tetrahydrofuran at ambient temperature was added 0.52 mL (4.0 mmol) of 3-ethoxyaniline and the resulting solution was stirred for 20 min. To this reaction mixture was slowly added a solution of 0.48 g (4.0 mmol) of 4-fluorobenzonitrile in 2.0 mL of tetrahydrofuran. The resulting mixture was stirred at ambient temperature for 5 hrs and then poured into brine (25 mL) and dichloromethane (50 mL). The organic layer was separated and the aqueous layer was extracted with dichloromethane (25 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to yield the title compound as yellow solid which was used without further purification. LC/JMS 259.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759352B2
Source datasetuspto-grants-2010_07
ORD IDord-40ff4ad6fc7f46c0a35d88ac7629c940
Source noteuspto-grants-2010_07