HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-Dodecanoxy-2-triethylsilylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Iodododecane | HCID 20282 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | 4-Hydroxymethyl-2-triethylsilylfuran | HCID 15037035 | — |
| Product | 4-Dodecanoxy-2-triethylsilylfuran | HCID 19019857 | — |
Reaction Steps
A solution of 4-hydroxymethyl-2-triethylsilylfuran (Compound 1, 160 mg, 0.75 mmol) in tetrahydrofuran (0.5 ml) was added to a suspension of potassium hydride (33 mg, 0.83 mmol) in tetrahydrofuran (1 ml) at room temperature. When all the potassium hydride disappeared, 1-iodododecane (0.37 ml, 1.5 mmol) was added. Stirring was continued for 4 days at room temperature. The reaction mixture was quenched with water. Extraction (ethyl ether) and evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by flash chromatography on silica using 5% ethyl ether/hexane. Fractions with Rf of about 0.65 on evaporation gave the titled ether as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05298633 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-413aef5246c04bbdab4f6f30a2fe0bdb |
| Source note | uspto-grants-1994_03 |