HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-hydroxy-2-methyl-2H-1-benzopyran-3-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,5-Dihydroxybenzaldehyde | HCID 70949 | — |
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-hydroxy-2-methyl-2H-1-benzopyran-3-carboxaldehyde | HCID 19815628 | — |
Reaction Steps
The starting material is prepared as follows: A mixture of 2,5-dihydroxybenzaldehyde (5.0 g, 36.2 mmol), crotonaldehyde (3.8 g, 54.3 mmol), and potassium carbonate (10.0 g, 72.4 mmol) in 75 ml of 1,4-dioxane is heated at reflux for 6 hours. The mixture is cooled and poured into water. This is extracted (3×) with dichloromethane, and the combined organic layers are dried (MgSO4) and concentrated to dryness to give 6-hydroxy-2-methyl-2H-1-benzopyran-3-carboxaldehyde as a colored solid. Such is converted to 6-benzyloxy-2-methyl-2H-1-benzopyran-3-carboxaldehyde, m.p. 107°-109° C., which is in turn converted to 3-(N-hydroxyaminomethyl)-6-benzyloxy-2-methyl-2H-1-benzopyran as described above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05155130 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-4d28483d548d453398991708eab86c88 |
| Source note | uspto-grants-1992_10 |