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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737253Generated: November 1, 2026

Acetic Anhydride → 2-Methyl-thieno[3,2-d][1,3]oxazin-4-one

https://huagongshe.com/reaction/1737253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium AcetateHCID 517045—
Reactant3-Acetamidothiophene-2-carboxylic acidHCID 2807579—
Solvent1,4-DioxaneHCID 31275—
Product2-Methyl-thieno[3,2-d][1,3]oxazin-4-oneHCID 12669250119.4%

Reaction Steps

To a mixture of 3-acetamidothiophene-2-carboxylic acid (15.1 g, 75.67 mmol) and sodium acetate (6.45 g, 78.6 mmol) in dioxane (200 mL) was added acetic anhydride (71 mL, 75.7 mmol). The reaction was refluxed 2 hours, cooled to ambient temperature and partitioned between chloroform and water. Phases were separated and the aqueous layer was extracted with chloroform. The combined organic phase was washed with water and brine, dried over magnesiuym sulfate and concentrated to leave 15.1 g of 2-methyl-thieno[3,2-d][1,3]oxazin-4-one as a brown oil which slowly solidified.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962457
Source datasetuspto-grants-1999_10
ORD IDord-f1a00c7973374f43b165a2830c6b3352
Source noteuspto-grants-1999_10