Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 21270165 | HCID 21270165 | — |
| Product | HCID 57890277 | HCID 57890277 | 42% |
Reaction Steps
3-(3,4-Dimethoxy-phenyl)-7-hydroxy-8-methylchromen-4-one (94.8 g) was suspended in acetic anhydride (450 mL) under a nitrogen atmosphere. Pyridine (23 mL) was added and the reaction mixture was heated to reflux for 1 hour. The pot was cooled overnight at −18° C. to produce a crystalline solid within the reaction mixture. This was filtered and the solid was washed with the filtrate and additional water (500 mL) to yield a brown solid. Further washing with ethanol produced a white crystalline solid. The solid was dried overnight in a desiccator to yield 7-acetoxy-3-(3,4-dimethoxyphenyl)-8-methylchromen-4-one (44.7 g, 42%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700644B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-10fe1bb152f142d4a1447397fb6d0f55 |
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| Source note | uspto-grants-2010_04 |
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