HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-Ethylsulfanyl-3-methoxy-3-methyl-but-1-yne
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Ethylsulfanyl-2-methyl-but-3-yn-2-ol | HCID 58979596 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Ethylsulfanyl-3-methoxy-3-methyl-but-1-yne | HCID 58979604 | — |
Reaction Steps
1-Ethylsulfanyl-2-methyl-but-3-yn-2-ol (0.29 g, 2.0 mmol) was added to a mixture of sodium hydride (60% dispersion in mineral oil, 88 mg, 2.2 mmol) in dimethylformamide (5 mL) under argon. Iodomethane (0.12 mL, 2.0 mmol) was then added to the reaction mixture via syringe and the mixture allowed to stir overnight. The mixture was poured onto water and extracted twice with diethyl ether. The diethyl ether extracts were washed with water and brine, dried over magnesium sulfate, filtered, and evaporated to yield a yellow oil. The oil was purified by column chromatography eluting with dichloromethane to yield the title compound as a clear liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07705147B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-bdc25266d2b84feeabcd22c105de5602 |
| Source note | uspto-grants-2010_04 |