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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737265Generated: November 1, 2026

Acetic Anhydride → HCID 15425486, compound

https://huagongshe.com/reaction/1737265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium AcetateHCID 517045—
ReactantHCID 18350683HCID 18350683—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 15425486HCID 1542548696.1%

Reaction Steps

A mixture of 3-acetamidothiophene-4-carboxylic acid (1.6 g, 8.65 mmol), dioxane (40 mL), acetic anhydride (10.2 mL, 86.5 mmol), and sodium acetate (0.75 g, 9.08 mmol) was refluxed overnight. The reaction was cooled and concentrated. The residue was partitioned between ethyl acetate and water. Phases were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with water and brine, dried over sodium sulfate, and concentrated to afford 1.39 g (96%) of 2-methyl-thieno[3,4-d][1,3]oxazin-4-one as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962457
Source datasetuspto-grants-1999_10
ORD IDord-a55d8756df0a466a9578cd028ebaa75f
Source noteuspto-grants-1999_10