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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434834Generated: October 29, 2026

Acetamide → HCID 13092002, compound

https://huagongshe.com/reaction/434834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamideHCID 178—
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantDiethyl CarbonateHCID 7766—
ReactantHCID 13093555HCID 13093555—
ReactantPotassium tert-butoxideHCID 23665647—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
ProductHCID 13092002HCID 13092002—

Reaction Steps

Potassium tert.-butoxide (539 mg., 4.8 mmoles) was dissolved in ethanol (2.12 g., 2.65 ml., 4.6 moles). Diethyl carbonate (625 mg., 5.3 mmoles) and then 2-(5-chloro-2-methoxyphenyl)-2-hydroxyacetamide (1.0 g., 4.6 mmoles) were added and the mixture was stirred for a few minutes to achieve solution, and then heated to reflux for 16 hours, at which time tlc (1:1 ethyl acetate:chloroform) indicated some unreacted starting material. Addition of more diethyl carbonate (625 mg.) and potassium tert-butoxide (100 mg.) and a further 2.5 hours of reflux did not appear to significantly reduce the level of starting acetamide. The reaction mixture was cooled to room temperature, poured into excess, iced 1 N hydrochloric acid and extracted with three portions of chloroform. The combined chloroform extracts were extracted with excess 5% sodium bicarbonate in two portions. The combined bicarbonate extracts were poured slowly into excess 1 N hydrochloric acid to precipitate 5-(5-chloro-2-methoxyphenyl)oxazolidine-2,4-dione (430 mg. 39%; m.p. 179°-181° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04399296
Source datasetuspto-grants-1983_08
ORD IDord-93835edccac44148bbe33ba3a551e946
Source noteuspto-grants-1983_08