HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 4-Acetyl-6-methoxy-1H-2-benzopyran-1,3(4H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | L-Selenocysteine | HCID 25076 | — |
| Reactant | 2-(Carboxymethyl)-4-methoxybenzoic acid | HCID 11816626 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Acetyl-6-methoxy-1H-2-benzopyran-1,3(4H)-dione | HCID 57893130 | — |
Reaction Steps
Following a literature procedure (Ind. J. Chem. Sec. B, 1986, 25B, 640-643), 2-carboxymethyl-4-methoxybenzoic acid (41; 1.0 g; 4.8 mmol) was dissolved in a mixture of pyridine (1.4 mL) and acetic anhydride (8.6 mL; 9.3 g; 91 mmol) then stirred for 3 h during which time a solid had formed. The suspension was diluted with diethyl ether, filtered and the filter cake washed with diethyl ether. Yield: 905 mg (81%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518874B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-9dbcd17b4c6246988894397593cd8cad |
| Source note | uspto-grants-2013_08 |