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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266447Generated: November 1, 2026

Iodoethane → HCID 15325841, compound

https://huagongshe.com/reaction/266447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactantn,n,2-triethylbenzamideHCID 225866—
ReactantCID 53628100HCID 178418400—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
ProductHCID 15325841HCID 1532584143%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4.74 ml (0.031 mol) of tetramethylethylenediamine in 300 ml of THF (passed through alumina prior to use) was added 5.8 g (0.03 mol) of 2-ethyl-N,N-diethylbenzamide. The solution was cooled to -78° C. and treated with a solution of 34.9 ml (0.031 mol) of a 0.9M solution of s-butyl lithium in cyclohexane. When addition was complete, the mixture was stirred for twenty minutes and then treated with a solution of 3.2 ml (0.04 mol) of ethyl iodide while maintaining the temperature at -78 ° C. The temperature was then allowed to rise to ambient temperature and the mixture stirred for about sixteen hours and then poured into water. The resulting oil was separated and chromatographed on silica gel, eluting with 10% ethyl acetate/hexane to give 2.86 g (43%) of 2-sec.-butyl-N,N-diethylbenzamide as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650422
Source datasetuspto-grants-1997_07
ORD IDord-d2c3045ee56f4f39abdbab18e209dc4b
Source noteuspto-grants-1997_07