Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 6-Methoxy-1,2,3,4-tetrahydronaphthalen-2-one | HCID 75582 | — |
| Reactant | Ethylorthoformate | HCID 53630039 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | 3-Ethoxy-7-methoxy-1,2-dihydronaphthalene | HCID 21844235 | — |
Reaction Steps
33.5 g of 6-methoxy-2-tetralone was dissolved in 27.6 ml of ethanol, followed by subsequently adding 37.8 ml of ethyl orthoformate and one drop of concentrated sulfuric acid. The mixture thus prepared was stirred at 100° C. for 4 hours. After distilling off the solvent under a reduced pressure, the resulting residue was subjected to silica gel column chromatography using chloroform as an eluant. Fractions of interest were pooled and concentrated to collect precipitated crystals, thereby obtaining 5.82 g of 3,4-dihydro-2-ethoxy-6-methoxynaphthalene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05866577 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-4cdbf89a82754d4d83f635c2a5599fc0 |
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| Source note | uspto-grants-1999_02 |
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