HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Methyl-N-(5-methylthiophen-2-yl)propanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | N-(3-Carbomethoxy-5-methyl-2-thienyl)-2-methylpropanamide | HCID 23341602 | — |
| Reactant | Lithium iodide (LiI), dihydrate | HCID 23688289 | — |
| Solvent | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Product | 2-Methyl-N-(5-methylthiophen-2-yl)propanamide | HCID 23341628 | 86.7% |
Reaction Steps
N-(3-Carbomethoxy-5-methyl-2-thienyl)-2-methylpropanamide (4.1 g, 0.017 mol), prepared by the method of Example 48, was dissolved in hot collidine (10 ml) and added to a mixture of lithium iodide dihydrate (10.1 g, 0.06 mol) in collidine (20 ml) kept under nitrogen. The reaction mixture was stirred under reflux for 48 hours, cooled and equilibrated between ether (3×50 ml) and 5 N-hydrochloric acid (50 ml). The ethereal solution was washed with water (25 ml), dried (Na2SO4) and evaporated to yield the required product as an off-white solid (2.7 g, 47%) m.p. 96°-97° C. The product was identical to the product described in Example 38.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04222946 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-20f01006fd414d4dab39ec0fa82bcd2b |
| Source note | uspto-grants-1980_09 |