HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → (S)-Glycidyl N-methyl-N-Methanesulfonyl-p-Aminophenyl Ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (S)-N-(4-(Oxiran-2-ylmethoxy)phenyl)methanesulfonamide | HCID 11322479 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (S)-Glycidyl N-methyl-N-Methanesulfonyl-p-Aminophenyl Ether | HCID 86593513 | 78% |
Reaction Steps
A solution of compound 3-S (0.243 g, 1 mmol) and potassium carbonate (0.166 g, 1.2 mmol) in 20 ml acetone was stirred for 1 hour at room temperature, then methyl iodide (0.142 g, 0.062 ml, 1 mmol) was added dropwise at room temperature. After stirring for 8 hours, the reaction was filtered and the solvent evaporated to furnish a white solid that was used directly in the next step (0.2 g, 78% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07375136B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-5355fc12a8214739a0cfcad600625718 |
| Source note | uspto-grants-2008_05 |