HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-ol → 1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-ol | HCID 70665277 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-one | HCID 10911758 | 80.5% |
Reaction Steps
To a solution of 1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-ol (3.0 g, 12.2 mmol) in DCM (50 mL) was added DMP (10.0 g, 24.4 mmol). The resulting solution was stirred for 30 min at room temperature and then the reaction mixture was poured into NaHCO3/NaS2O3 solution and stirred for overnight, extracted with DCM (3×150 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo to give a residue. The residue was purified by silica gel column chromatography (3% ethyl acetate in petroleum ether) to afford 1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-one as a light yellow oil (2.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912188B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-7be7eb5c217e4966b6cd620c7721466e |
| Source note | uspto-grants-2014_12 |