Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 12952273 | HCID 12952273 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 12952275 | HCID 12952275 | 97.9% |
Reaction Steps
To 8.9 g of 7-bromo-2-hydroxy-1,2,3,4-tetrahydro-9-xanthone obtained in Example 67 were added 6.2 g of anhydrous acetic acid and 40 ml of pyridine. The mixture was stirred for 4 hours at 60° C., and after completion of the reaction, the solvent was removed by distillation. The resulting crystals were recrystallized from ethanol to obtain 9.9 g (yield: 97.9%) of 2-acetoxy-7-bromo-1,2,3,4-tetrahydro-9-xanthone as colorless needle-like crystals having a melting point of 177.5° to 178° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04290954 |
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| Source dataset | uspto-grants-1981_09 |
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| ORD ID | ord-af5d92e6583b4f98b8213033bfad71c8 |
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| Source note | uspto-grants-1981_09 |
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