HuagongsheHuagongshe Chemistry Print Report · For research reference only
5'-Bromo-2'-hydroxyacetophenone → 6-bromo-2-(tetrahydro-2H-pyran-3-yl)chroman-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5'-Bromo-2'-hydroxyacetophenone | HCID 95991 | — |
| Reactant | Oxane-3-carbaldehyde | HCID 10129928 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-bromo-2-(tetrahydro-2H-pyran-3-yl)chroman-4-one | HCID 58424147 | 20% |
Reaction Steps
A mixture of 1-(5-bromo-2-hydroxyphenyl)ethanone (39 g, 181.8 mmol), tetrahydro-2H-pyran-3-carbaldehyde (20 g, 181.8 mmol) and borax (69.3 g, 181.8 mmol) in ethanol (240 mL) and H2O (400 mL) was refluxed for one day. The reaction mixture was cooled, diluted with an equal volume of H2O and extracted with ethyl acetate. The organic layer was dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to give 6-bromo-2-(tetrahydro-2H-pyran-3-yl)chroman-4-one (10 g, 20%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08921359B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-2fb87bf457da4e13973f024e09ca42e9 |
| Source note | uspto-grants-2014_12 |