HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 2-((tert-butoxycarbonyl)amino)-3-cyclohexylpropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Boc-DL-Cha-OH | HCID 2817530 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-((tert-butoxycarbonyl)amino)-3-cyclohexylpropanoate | HCID 4264602 | 97.9% |
Reaction Steps
To a solution of 2-tert-butoxycarbonylamino-3-cyclohexyl-propionic acid (3.0 g, 11.1 mmol) and potassium carbonate (1.5 g, 11.1 mmol) in N,N-dimethylformamide (20 mL) was added methyl iodide (0.795 μL; 12.1 mmol). The reaction mixture was stirred at room temperature overnight. To the reaction mixture was added ethyl acetate (100 mL) and the solution was washed with water (3×100 mL). The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated to give the title intermediate as an oil (3.1 g) which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08268863B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-2de1330834d74e1ea6f8b23f4a924318 |
| Source note | uspto-grants-2012_09 |