HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-(1-Methoxytridecyl)-2-trimethylsilylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(1-Hydroxytridecyl)-5-trimethylsilylfuran | HCID 15663268 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1-Methoxytridecyl)-2-trimethylsilylfuran | HCID 15037058 | — |
Reaction Steps
A mixture of 4-(1-hydroxytridecyl)-2-trimethylsilylfuran (318.5 mg, 0.9 mmol), sodium hydride (60% dispersion in oil; 150 mg, 3.8 mmol) and iodomethane (0.29 ml, 4.7 mmol) in tetrahydrofuran (7 ml) was refluxed for 16 hr. On cooling, the mixture was diluted with ethyl ether (20 ml), quenched with methanol (2 ml) and washed with water. Evaporation of the dried (magnesium sulfate) organic phase gave a deep yellow oil, identified as 4-(1-methoxytridecyl)-2-trimethylsilyfuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05134128 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-1f0659989c194f73a29d9f4455fa5925 |
| Source note | uspto-grants-1992_07 |