Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | HCID 58712184 | HCID 58712184 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58712145 | HCID 58712145 | — |
Reaction Steps
To 1-(5-ethyl-2,4-dihydroxy-phenyl)-2-naphthalen-2-yl-ethanone (c, 0.50 g) was added a mixture of pyridine (2 mL), trimethyl orthoformate (2 mL) and piperidine (2 drops), and the mixture was heated at 120° C. for 12 h. The mixture was cooled to room temperature, diluted with EtOAc (100 mL) then washed with 1 N HCl (100 mL). The organic layer was washed with water and dried. The oil obtained on concentration of the organic layer was crystallized in EtOAc/hexanes to give 6-ethyl-7-hydroxy-3-naphthalen-2-yl-chromen-4-one (d, 0.36 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598366B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-d589ea03042e415d9b70f3a402cf96b0 |
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| Source note | uspto-grants-2013_12 |
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