HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-dihydro-2H-pyran → HCID 66939482, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 56706473 | HCID 56706473 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66939482 | HCID 66939482 | 99.2% |
Reaction Steps
To a solution (50 mL) of the compound (7.0 g, 27 mmol) obtained in Example 64b in toluene were added dihydropyran (4.9 mL, 54 mmol) and conc. sulfuric acid (3 drops), and the mixture was stirred at room temperature overnight. The reaction mixture was neutralized with saturated aqueous sodium hydrogen carbonate, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The resulting crude title compound was purified by column chromatography (hexane-hexane/ethyl acetate=80/20) to give the title compound (9.2 g, 99%) as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461348B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-27c032fb96394b2d8c200def65e3c00f |
| Source note | uspto-grants-2013_06 |