HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613995Generated: October 28, 2026
Water → N-(Butan-2-yl)-N-(4-methyl-1,3-oxazol-2-yl)butanamide
https://huagongshe.com/reaction/613995
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Butanamide, N-(1-methylpropyl)- | HCID 346252 | — |
| Reactant | 4-Methyl-2-methylsulphinyloxazole | HCID 54159470 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(Butan-2-yl)-N-(4-methyl-1,3-oxazol-2-yl)butanamide | HCID 12556894 | — |
Reaction Steps
N-s-Butyl-butyramide (0.99 g, 0.0069 m) in dry dioxan (10 ml) was cooled to 10° C. under nitrogen during the dropwise addition of a 1.445 M solution of n-butyl lithium (4.8 ml, 0.0069 m). The mixture was stirred for 15 minutes at 10° C. and then 4-methyl-2-methylsulphinyloxazole (1.0 g, 0.0068 m) in dry dioxan (10 ml) was added and the mixture allowed to warm to room temperature. It was stirred for 3 hours and then hydrolysed with water. The solvent was removed in vacuo and the ether extract of the residue was chromatographed on silica using ether. The resulting compound (title product) was distilled in vacuo as a colourless oil 0.95 g, b.p. 75°-76° C./0.5 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04143047 |
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| Source dataset | uspto-grants-1979_03 |
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| ORD ID | ord-a18a9eefe37a4813b627d872e5a8ab35 |
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| Source note | uspto-grants-1979_03 |
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