Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | HCID 11543545 | HCID 11543545 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11687479 | HCID 11687479 | 49% |
Reaction Steps
To a 50 mL round-bottomed flask fitted with condenser and magnetic stirrer was added 2-(2-amino-4-methoxyphenyl)-4H-chromen-4-one (770 mg, 2.88 mmol), hydroiodic acid (10 mL) and acetic acid (4 mL). The reaction mixture was heated to 110° C. for 8 h. The reaction mixture was cooled to rt and diluted with water. The precipitate was filtered off, washed with water and dried to give the crude compound, which was purified by column chromatography using 2% MeOH in CH2Cl2, to give 2-(2-amino-4-hydroxy-phenyl)-chromen-4-one (357 mg, 49%). MS (ES) m/z: 254.05 (M+1), 149.00, 134.01, and 121.00.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242130B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-7c0ab17e1be44d03b4f8f3c5c1517bd7 |
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| Source note | uspto-grants-2012_08 |
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