HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 2-(7-hydroxy-4-methyl-2-oxo-2H-chromen-3-YL)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-(7-hydroxy-4-methyl-2-oxo-2H-chromen-3-yl)acetic acid | HCID 5393149 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-(7-hydroxy-4-methyl-2-oxo-2H-chromen-3-YL)acetate | HCID 20282952 | 92% |
Reaction Steps
7-Hydroxy-4-methylcoumarin-3-acetic acid (1) (1 gm, 4.3 mmol) was suspended in anhydrous ethanol (15 mL), concentrated sulfuric acid (1.5 mL) was added and the mixture was heated at reflux for 1 hour. The reaction mixture was cooled to room temperature, diluted with ethyl acetate (100 mL), washed with 5% NaHCO3 (5×50 mL), water (2×50 mL), saturated NaCl (2×50 mL) dried with sodium sulfate, filtered and the filtrate was evaporated under reduced pressure to give 1.04 gm (4.0 mmol, 92% yield of 2 as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05731158 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-3da89dd6f0cf4b19a43b09c6563de2f4 |
| Source note | uspto-grants-1998_03 |