HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → (7-Acetoxy-2-oxo-2H-chromen-4-yl)-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 7-Hydroxycoumarin-4-acetic acid | HCID 5338490 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (7-Acetoxy-2-oxo-2H-chromen-4-yl)-acetic acid | HCID 12514017 | 30% |
Reaction Steps
To 9 (1 g, 4.53 mmol) was added 25 ml of acetic anhydride and 5 ml of pyridine, and the reaction was allowed to stir at RT for 30 minutes. Upon removal of solvent in vacuo, the residue was taken into ethyl acetate and washed with 1 N HCl (2×30 ml), water (2×30 ml) and brine (2×30 ml). The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo to afford 10 (30% yield). 1H NMR (300 MHz, CDCl3) δ 7.71 (d, J=8.9 Hz, 1H), 7.23 (d, J=5.6 Hz, 1H), 7.24 (s, 1H), 6.47 (s, 1H), 2.94 (s, 2H), 2.33 (s, 3H). MS (ESI): m/z 263.0 [(M+H)]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07449558B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-218ce70186b0469dba86d78134e3ec95 |
| Source note | uspto-grants-2008_11 |