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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591103Generated: November 2, 2026

Diethylamine → HCID 178464205, compound

https://huagongshe.com/reaction/1591103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 178510663HCID 178510663—
SolventDichloromethaneHCID 6344—
SolventDiglymeHCID 8150—
ProductHCID 178464205HCID 178464205—

Reaction Conditions

Temperature0 °C

Reaction Steps

Diethylaminosulphur trifluoride (1.5 ml) was added dropwise to a stirred suspension of 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 numberUS05206257
Source datasetuspto-grants-1993_04
ORD IDord-0d357d1937af493d91cc192f25402096
Source noteuspto-grants-1993_04