HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-[[N-(tert-butyloxycarbonyl)-N-methylamino]methyl]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-Boc-2-aminomethylpyridine | HCID 12069550 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[[N-(tert-butyloxycarbonyl)-N-methylamino]methyl]pyridine | HCID 19606213 | 70.6% |
Reaction Steps
A solution of 19.8 g (95 mmol) of 2-(N-(t-butyloxycarbonyl)aminomethyl)pyridine in anhydrous tetrahydrofuran was cooled under N2 atmosphere to 0° C. and treated with 4.95 g (124 mmol) of sodium hydride (60% dispersion in oil). The solution was stirred for 15 min, treated dropwise with 7.1 ml (114 mmol) of methyl iodide, stirred at ambient temperature for 2 h, and quenched cautiously with water. The resulting mixture was partitioned between ether and water, dried over Na2SO4, and concentrated in vacuo. Chromatography on silica gel provided 14.9 g (70%) of the desired compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05461067 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-f35371a81db141818b00ca360b708355 |
| Source note | uspto-grants-1995_10 |