HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-phenoxy-2H-1-benzopyran-3-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acrolein | HCID 7847 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Hydroxy-5-phenoxybenzaldehyde | HCID 14971258 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-phenoxy-2H-1-benzopyran-3-carboxaldehyde | HCID 14971265 | — |
Reaction Steps
A mixture of 5-phenoxysalicylaldehyde (15.0 g, 70.0 mmol, see example 2d) and potassium carbonate (19.4 g, 140.0 mmol) in 250 ml of 1,4-dioxane is treated with acrolein (4.32 g, 77.0 mmol) under nitrogen. The mixture is heated at reflux for 6 hours. Water is added and the mixture is extracted with dichloromethane. The organic layer is dried (MgSO4) and evaporated. The residue is purified by flash chromatography (silica gel, 10% EtOAc/hexane) to give 6-phenoxy-2H-1-benzopyran-3-carboxaldehyde, as a fluorescent solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05155130 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-6ea02f94213a4e928ef2fb095314ef05 |
| Source note | uspto-grants-1992_10 |