HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → N,2-Diethyl-N-(4-methyl-1,3-oxazol-2-yl)butanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 12556852 | HCID 12556852 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N,2-Diethyl-N-(4-methyl-1,3-oxazol-2-yl)butanamide | HCID 21323622 | 51.1% |
Reaction Steps
Sodium hydride (2.8 g. of a 50% dispersion in oil, 0.058 mol) was added in small portions to a stirred solution of 2-(2-ethylbutyramido)-4-methyloxazole (8.0 g., 0.041 mol) in dimethylformamide (100 ml.) at -5° to 0° C. The mixture was stirred for 2 hours at room temperature and then ethyl iodide (4.7 ml. 0.058 mol) was added. The mixture was stirred for a further 2 hours at room temperature and then poured onto ice-water (250 ml.) and extracted with ether (3 × 100 ml.). The extract was washed with dilute hydrochloric acid, then with sodium chloride solution, dried over sodium sulphate and evaporated. The residue was distilled under vacuum to give the product 4.7 g. (51%) b.p. 71-72° C/0.3 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04150143 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-07097c77bf794604bc3b2c694c5a8945 |
| Source note | uspto-grants-1979_04 |