HuagongsheHuagongshe Chemistry Print Report · For research reference only
Kojic Acid → 5-Hydroxy-2-{[(oxan-2-yl)oxy]methyl}-4H-pyran-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Kojic Acid | HCID 3840 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Product | 5-Hydroxy-2-{[(oxan-2-yl)oxy]methyl}-4H-pyran-4-one | HCID 13711789 | 29,265.199% |
Reaction Steps
To a suspension of 14.3 g of kojic acid in 57 mL of tetrahydrofuran, 11 mL of 3,4-dihydro-2H-pyran and 77 mg of p-toluenesulfonic acid monohydrate were added, and the mixture was stirred for 6 hours at room temperature. To the mixture, 1 mL of a 0.5 mol/L sodium hydroxide aqueous solution was added, and the solvent was evaporated under reduced pressure to give 26.8 g of 5-hydroxy-2-((tetrahydro-2H-pyran-2-yloxy)methyl)-4H-pyran-4-one as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354426B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-795ea3a9880f4007aa6b25dec1c8c733 |
| Source note | uspto-grants-2013_01 |