HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-Acetylamino-4-(naphth-1-yl)oxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-4-(naphth-1-yl)oxazole | HCID 10307957 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Acetylamino-4-(naphth-1-yl)oxazole | HCID 59796840 | — |
Reaction Steps
To a cooled (ice/salt bath) mixture of 2-amino-4-(naphth-1-yl)oxazole (1)(0.5 g) and triethylamine (0.8 ml) in anhydrous dichloromethane (5 ml) was added dropwise acetyl chloride (0.2 ml) over a minute. The resulting mixture was warmed to room temperature and left overnight. Further acetyl chloride (0.1 ml) was added and the mixture left for a further hour. Dichloromethane (40 ml) and few drops of methanol were added. The mixture was washed twice with brine, dried with sodium sulphate, filtered and evaporated in vacuo. The title compound (9) (0.35 g; m.p. 188-190° C.) was obtained following silica gel column chromatography of the residue in 2% methanol in chloroform.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07429607B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-4a542a07cdbf48b783167e4decab0fd8 |
| Source note | uspto-grants-2008_09 |