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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266448Generated: November 1, 2026

Iodoethane → HCID 15325842, compound

https://huagongshe.com/reaction/266448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantHCID 11068228HCID 11068228—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15325842HCID 1532584225.1%

Reaction Steps

To a solution of 9.3 ml (0.058 mol) of tetramethyl-ethylenediamine in 340 ml of THF at -78° C was added 52 ml of a 1.1M solution (0.057 mol) of s-butyl lithium in THF. The solution was then treated with a solution of 11.37 g (0.052 mol) of 2-propyl-N,N-diethylbenzamide in 75 ml of THF at -78° C. and the solution stirred for fifteen minutes and then treated with a solution of 8.3 ml of (0.104 mol) of ethyl iodide in THF. The solution was stirred for an hour and a half at -78° C. and then quenched by the addition of saturated ammonium chloride added dropwise at -78° C. The mixture was then allowed to warm to ambient temperature, diluted with diethyl ether, washed first with dilute hydrochloric acid, then with water, then with saturated sodium bicarbonate, then with brine dried and taken to dryness to give 12.91 g of crude product which was chromatographed on silica gel, eluting with 10% ethyl acetate/hexane to give 3.23 g (25%) of 2-(3-pentyl)-N,N-diethylbenzamide as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650422
Source datasetuspto-grants-1997_07
ORD IDord-136e7e482d9042979c3b6cabb1b4e4ef
Source noteuspto-grants-1997_07