Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrolein | HCID 7847 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 58439092 | HCID 58439092 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86657638 | HCID 86657638 | — |
Reaction Steps
To a solution of 2-hydroxy-4-[(2-methoxy-4-propylphenoxy)methyl]benzaldehyde (120 mg) in dioxane (2.4 mL) were added K2CO3 (55.2 mg) and acrolein (0.267 mL) at 25° C. The reaction mixture was warmed to 100° C., followed by stirring at 100° C. for 15 hours. The reaction mixture was left to be cooled to 25° C., and then filtered through celite, and the filtrate was concentrated. The residue was purified by silica gel column chromatography (automatic purification device, hexane:EtOAc=100:0 to 80:20) to obtain 7-[(2-methoxy-4-propylphenoxy)methyl]-2H-chromene-3-carbaldehyde (104.2 mg) as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193378B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-567d53b2e03a457d995931f1e3cb573d |
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| Source note | uspto-grants-2012_06 |
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