HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-acetyl-6-phenoxy-2H-1-benzopyran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Hydroxy-5-phenoxybenzaldehyde | HCID 14971258 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-acetyl-6-phenoxy-2H-1-benzopyran | HCID 14971313 | — |
Reaction Steps
The starting material is prepared as follows: 5-Phenoxysalicylaldehyde (6.17 g, 28.8 mmol) is dissolved in 100 ml of 1,4-dioxane and treated with potassium carbonate (7.96 g, 57.6 mmol) and methyl vinyl ketone (3.03 g, 43.2 mmol) under nitrogen. The mixture is heated at reflux for 3 hours. Water is added and three extractions with dichloromethane are carried out. The organic extracts are combined, dried (MgSO4) and evaporated. Purification by flash chromatography (silica gel, 15% EtOAc/hexane) yields 3-acetyl-6-phenoxy-2H-1-benzopyran as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05155130 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-e417788173cd473093af3bfed4b09662 |
| Source note | uspto-grants-1992_10 |