Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 86621969 | HCID 86621969 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86621968 | HCID 86621968 | — |
Reaction Steps
To a solution of methyl 4-(3-methylphenyl)-2-oxo-2H-chromene-7-carboxylate (610 mg, 2.1 mmol) in THF (21 mL) a solution of lithium hydroxide (10.3 mL, 10.3 mmol) was added. The solution was then heated at 65° C. for 2 hours. After cooling, volatiles were removed under reduced pressure and the residue obtained was diluted with THF (20 mL) and 2N HCl (40 mL). After 1 h stirring, the solid formed was collected by filtration to afford the title compound. 1H NMR (400 MHz, DMSO-d6): 13.5 (bs, 1H), 7.90 (d, 1H), 7.87 (dd, 1H), 7.59 (d, 1H), 7.48 (t, 1H), 7.43-7.33 (m, 3H), 6.55 (s, 1H), 2.41 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960409B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-85e15041d214485bb84b1597b592e937 |
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| Source note | uspto-grants-2011_06 |
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