HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-Hexyl-N-(3-methyl-1,2,4-oxadiazol-5-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | N-Hexyl-3-methyl-1,2,4-oxadiazol-5-amine | HCID 54080718 | — |
| Product | N-Hexyl-N-(3-methyl-1,2,4-oxadiazol-5-yl)acetamide | HCID 20393669 | — |
Reaction Steps
5-n-Hexylamino-3-methyl-1,2,4-oxadiazole (4.6 g, 0.025 mole) was dissolved in acetic anhydride (25 ml) and refluxed for 3 hours and then evaporated down to dryness under vacuum. The residue was taken up in CHCl3 (50 ml) and washed twice with 2N HCl and twice with a saturated solution of NaHCO3 and dried over MgSO4. (b.p. 113°-114° C./1.0 mmHg.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04163048 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-8fa3a79bcfd5458fbb5cf4034fa69bda |
| Source note | uspto-grants-1979_07 |