HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → methyl N-(tert-butoxycarbonyl)-N-(2-cyanoethyl)-2-methylalaninate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 2-((tert-Butoxycarbonyl)(2-cyanoethyl)amino)-2-methylpropanoic acid | HCID 57523644 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl N-(tert-butoxycarbonyl)-N-(2-cyanoethyl)-2-methylalaninate | HCID 57523645 | 97% |
Reaction Steps
62 g (0.23 mol) of N-(tert-butoxycarbonyl)-N-(2-cyanoethyl)-2-methylalanine were dissolved in 350 ml of DMF and 50 g of KHCO3 were added. Few minutes after, 30 ml of methyl iodide (MeI) were dropped and the mixture was stirred at room temperature for 6 hours. Then a further 15 ml of MeI were added. The mixture was left at room temperature overnight. After dilution with 1.5 l of water, the solution was extracted with ethyl acetate (3 times). The organic phases were washed with a small amount of water, dried over sodium sulfate, evaporated and dried at the mechanical pump. 60.5 g (97%) of methyl N-(tert-butoxycarbonyl)-N-(2-cyanoethyl)-2-methylalaninate were thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08557857B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-dd59f248017346a78a5105b9afae474a |
| Source note | uspto-grants-2013_10 |