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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769302Generated: October 31, 2026

Diethylamine → HCID 178464205, compound

https://huagongshe.com/reaction/1769302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 178510663HCID 178510663—
SolventDichloromethaneHCID 6344—
SolventDiglymeHCID 8150—
ProductHCID 178464205HCID 17846420516%

Reaction Conditions

Temperature0 °C

Reaction Steps

5-cyano-2-(2,6-dichloro-4-trifluoromethylphenyl)-imidazole-4-carboxylic acid (1.4 g, 0.004 mol) in 2-methoxyethyl ether (11 ml) whilst maintaining the temperature at about 0° C. Potassium fluoride (0.67 g, 0.0115 mol) was added and the mixture was stirred at 0° C. for 0.5 hours, and added slowly to a solution of diethylamine (8.8 g, 12.5 ml, 0.12 mol) in dichloromethane (75 ml) whilst maintaining the temperature in the range 0°-5° C. The mixture was stirred at 0°-5° C. for 1 hour and at room temperature for 0.5 hours. The mixture was washed with saturated aqueous sodium bicarbonate solution (50 ml), dried over anhydrous sodium sulphate and evaporated to dryness. The residue was purified by mplc on silica eluting with a mixture of ethyl acetate and dichloromethane (1:2) to give N,N-diethyl 5-cyano-2-(2,6-dichloro-4-trifluoromethylphenyl)imidazole-4-carboxamide (0.26 g) m.p. 195°- 197° C. as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380865
Source datasetuspto-grants-1995_01
ORD IDord-bc55a865441e445ba9a6f8508305ce8a
Source noteuspto-grants-1995_01