HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 7-Hydroxy-4-methoxymethyl-8-methylcoumarin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-(chloromethyl)-7-hydroxy-8-methyl-2H-chromen-2-one | HCID 5423877 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 7-Hydroxy-4-methoxymethyl-8-methylcoumarin | HCID 18421448 | — |
Reaction Steps
A mixture of 4-chloromethyl-7-hydroxy-8-methylcoumarin (2.00 g, 8.90 mmol) and sodium methoxide (12.0 g, 222 mmol) in methanol (400 mL) was refluxed overnight. The solution was allowed to cool to room temperature, acidified to pH 0-1 with 5-6N HCl in isopropanol and evaporated. The residue was azeotroped with toluene several times to give crude product 7-hydroxy-4-methoxymethyl-8-methylcoumarin, a yellow oil. 1H NMR (CD3OD): δ 7.38 (d, J=8.5 Hz, 1H), 6.82 (d, J=8.8 Hz, 1H), 6.29 (s, 1H), 4.66 (s, 2H), 3.51 (s, 3H), 2.26 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06133460 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-9ce182e687094fd589fdb936d1fab731 |
| Source note | uspto-grants-2000_10 |