HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-(tert-Butoxycarbonyl)-N-methyl-D-alanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | BOC-D-alanine | HCID 637606 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(tert-Butoxycarbonyl)-N-methyl-D-alanine | HCID 16211306 | — |
Reaction Steps
To 48 ml of a solution of Boc-D -Ala-OH (3.0 g, 15.9 mmol) in tetrahydrofuran (THF) was added 60% sodium hydride (1.9 g, 47.6 mmol) under ice-cooling and the mixture was stirred for 10 minutes. Then, methyl iodide (7.9 ml, 127 mmol) was added and the mixture was further stirred at room temperature for 22 hours. The reaction mixture was then concentrated under reduced pressure, ice-cooled, acidified with 10% citric acid-H2O, and extracted with ethyl acetate. The extract was washed with saturated NaCl-H2O, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was crystallized from hexane and the crystal crop was washed with hexane to provide the title compound. Yield 3.07 g (94.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05698670 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-b8bc3247e8784172a873f1c3fe794e9a |
| Source note | uspto-grants-1997_12 |