HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-Butyl-2-methyl-N-(1,3-oxazol-2-yl)propanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Hexanamide, 2,2-dimethyl- | HCID 181100 | — |
| Reactant | 2-Ethylsulphinyloxazole | HCID 21329745 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-Butyl-2-methyl-N-(1,3-oxazol-2-yl)propanamide | HCID 12556913 | — |
Reaction Steps
n-Butyl-isobutyramide(4.93 g, 0.0344 m) in dry diethyl ether (25 ml) was stirred at room temperature under nitrogen during the dropwise addition of a 1.445 M solution of n-butyl lithium (23.8 ml, 0.0344 m). The mixture was stirred for 15 minutes at room temperature and then 2-ethylsulphinyloxazole (5.0 g, 0.0344 m) in dry diethyl ether (25 ml) was added rapidly. The mixture was stirred at room temperature for 3 hours and then hydrolysed with water. The organic phase was washed several times with water, dried over magnesium sulphate and evaporated in vacuo to give a yellow oil. Distillation gave the title product as a colourless oil, b.p. (airbath) 120° C./0.5 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04143047 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-8e1a6507e8de45feae6fc24268fd9771 |
| Source note | uspto-grants-1979_03 |