HuagongsheHuagongshe Chemistry Print Report · For research reference only
Mexiletine → Mexiletine acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Mexiletine | HCID 4178 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 67701997 | HCID 67701997 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Mexiletine acetate | HCID 567741 | — |
Reaction Steps
In Step 1, 2-(2,6-dimethylphenoxy)-1-methyl-ethylamine (mexiletine) is converted to mexiletine acetamide. Mexiletine is treated with an acetylating agent, such as an acetyl chloride or acetic anhydride, in the presence of concentrated aqueous alkali and an organic solvent, e.g., ethyl acetate. The reaction temperature is maintained at about 0°-25° C., preferably below 10° C., for about 10 minutes to 3 hours, preferably about 35 minutes. Following completion of the reaction, the resulting N-[2-(2,6-dimethylphenoxy)-1-methylethyl]-acetamide is isolated by conventional techniques, and used as such in Step 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688830 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-8d671e650dfa4e4b80688111e6b099e7 |
| Source note | uspto-grants-1997_11 |