HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 12669250, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-Acetamidothiophene-2-carboxylic acid | HCID 2807579 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 12669250 | HCID 12669250 | 119.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06323208B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-82c2df153c004ea5b5d5c17398b9629d |
| Source note | uspto-grants-2001_11 |