HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Phenoxythiazol-4-yl)methanol → 2-Phenoxythiazole-4-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Phenoxythiazol-4-yl)methanol | HCID 13106143 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 2-Phenoxythiazole-4-carbaldehyde | HCID 13102642 | — |
Reaction Steps
A solution of (2-phenoxythiazol-4-yl)methanol (251 mg; 1.21 mmol) in anh. DCE (12 ml) was treated with MnO2 (843 mg; 9.69 mmol), and the resulting mixture was stirred at reflux, under nitrogen, for 1 h. After cooling to rt, the mixture was filtered over a pad of celite, and the separated solids were washed with DCM. The filtrate was then concentrated to dryness under reduced pressure affording 2-phenoxythiazole-4-carbaldehyde as a pale yellow oil. LC-MS (conditions A): tR=0.65 min.; [M+H]+: 206.04 g/mol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242970B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-c60ea672fb81455492d4d2b0a0a88ed2 |
| Source note | uspto-grants-2016_01 |