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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065298Generated: October 31, 2026

Hydrochloric Acid → N-acetyl-N-ethyl-2-(acetylthio)acetamide

https://huagongshe.com/reaction/1065298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantN-acetyl-2-(acetylthio)acetamideHCID 12837856—
ReactantHCID 178418361HCID 178418361—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductN-acetyl-N-ethyl-2-(acetylthio)acetamideHCID 20540298—

Reaction Steps

A solution of 11 g. (0.063 mole) of N-acetyl-2-(acetylthio) acetamide in 75 ml. of dry dimethylformamide was cooled to -30° C. and there was then added 3.02 g. (0.063 mole) of 50% sodium hydride. The reaction mixture was aged until hydrogen evolution ceased. There was then added 5.1 ml. (0.063 mole) of ethyl iodide after cooling the reaction mixture to -40° C., after which the reaction mixture was allowed to come to room temperature and age overnight. A precipitate formed. There was next added 5 ml. of acetic acid, then 100 ml. of ether, followed by 30 ml. of 2.5 N hydrochloric acid and 70 ml. of water. The ether layer was separated and the water layer was increased to about 400 ml. with water, after which it was extracted three times with 100 ml. of ether. The ether extract was dried over magnesium sulfate and concentrated to an oil of 7.2 g. Composition of the product was verified by NMR and mass spectrometry.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04329363
Source datasetuspto-grants-1982_05
ORD IDord-7676e7e1637d4765aa604197a5f78d27
Source noteuspto-grants-1982_05