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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501878Generated: October 25, 2026

Iodoethane → N-(3-(3-(Dimethylamino)-1-oxo-2-propenyl)phenyl)-N-ethylacetamide

https://huagongshe.com/reaction/501878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantHexaneHCID 8058—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantN-[3-(3-Dimethylaminoacryloyl)phenyl]acetamideHCID 53412415—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-(3-(3-(Dimethylamino)-1-oxo-2-propenyl)phenyl)-N-ethylacetamideHCID 53395302—

Reaction Steps

4.25 gm of Potassium tert-butoxide was added portion wise to a clear solution of 5 gm N-[3-[3-(Dimethylamino)-1-oxo-2-propenyl]-phenyl] acetamide in 50 ml dimethyl formamide. A solution of 5.25 gm Ethyl iodide in 20 ml dimethyl formamide was added drop wise over 3 hrs. at 35° C.-40° C. The reaction mass was stirred for 6 hrs and then quenched in 300 ml of water and extracted in dichloromethane. The organic layer was washed with water, dried over sodium sulphate and concentrated under vacuum to get oil, which was dissolved in 5 ml dichloromethane and 50 ml hexane was added to precipitate the product. The solids obtained was filtered and washed with hexane and dried in vacuum tray dryer at 35° C. for 6 hrs.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772394B2
Source datasetuspto-grants-2010_08
ORD IDord-a6c3cf3bcf2e4bd9bd54a0e991f91f63
Source noteuspto-grants-2010_08