HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-(2-Chloro-4-pyridinyl)-N-methylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-(2-chloropyridin-4-yl)acetamide | HCID 2049955 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-(2-Chloro-4-pyridinyl)-N-methylacetamide | HCID 45119279 | 600.9% |
Reaction Steps
A mixture of 10 g (59 mmol) N-(2-chloropyridin-4-yl)acetamide (commercially available), 9.8 g (17.6 mmol) pulverized KOH and 4.1 ml (6.4 mmol) methyl iodide in 60 ml acetone was stirred at room temperature for 2 h. After evaporation of all volatiles the residue was taken up in water and extracted with ethyl acetate. The combined organic layers were dried with MgSO4 and evaporated to yield 7.1 g (66%) of the title compound as off-white solid. MS: (m/e): 345.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07456175B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-52ac5c96003c4f889411ab8a90617c22 |
| Source note | uspto-grants-2008_11 |