Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | 4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol | HCID 11123315 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11391841 | HCID 11391841 | 56.1% |
Reaction Steps
To a stirred solution of triphenylphosphine (1.4154 g, 5.34 mmol) in anhydrous dichlormethane (20 mL) at room temperature under nitrogen was added imidazole (360 mg, 5.24 mmol), followed by iodide (1.2688 g, 4.95 mmol). The mixture was stirred for three minutes, a solution of 4-(tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol (708.6 mg, 4.16 mmol) in dichloromethane was added dropwise via spring. The resulting mixture was continued to be stirred for 1.5 hours. The mixture was filtered through a pad of Celite. And the solid was washed with dichloromethane. The combined organic filtration was concentrated under reduced pressure. The residue was separated with flash column chromatography on silica using 0-20% EtOAc/hexane to afford 654 mg of product in 56% yield. 1H-NMR (CDCl3): δ 4.77 (t, J=3.0 Hz, 1H), 4.33-4.18 (m, 2 H), 3.85-3.77 (m, 1 H), 3.70 (t, J=2.1 Hz, 2 H), 3.56-3.49 (m, 1 H), 1.85-1.62 (m, 6 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09126926B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-b7a0ff1c7d4f46c28cb39b5c48a85334 |
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| Source note | uspto-grants-2015_09 |
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