HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 22940672, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (3S)-3-[(tert-Butoxycarbonyl)amino]-3-phenylpropanoic acid | HCID 2734490 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22940672 | HCID 22940672 | — |
Reaction Steps
A solution of 15 mL of DMF charged with (3S)-3-[tert-butoxycarbonylamino]-3-phenylpropionic acid (8 mmol, 2.0 g), methyl iodide (15 mmol, 1.9 mL) and K2CO3 (15 mmol, 2.1 g), was stirred at RT for 16 h. The reaction mixture was poured into 50 mL of saturated NaHCO3, and the resulting solution was extracted with ether (3×50 mL). The combined organic phase was washed with 50 mL of H2O, dried with MgSO4, and the solvent removed under reduced pressure to yield the title compound as a slightly yellow solid. 1H NMR (500 MHz, CDCl3): δ 7.26–7.38 (m, 5 H), 5.49 (br s, 1H), 5.13 (br s, 1H), 3.65 (s, 3H), 2.80–2.96 (m, 2H), 1.45 (s, 9H). MS (ESI): m/z 302 (M+Na).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07153868B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-7a805e2d4cdc4652bcbe0917c3d01533 |
| Source note | uspto-grants-2006_12 |