HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615924Generated: October 31, 2026
(2-Phenoxythiazol-4-yl)methanol → 2-Phenoxythiazole-4-carbaldehyde
https://huagongshe.com/reaction/615924
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (2-Phenoxythiazol-4-yl)methanol | HCID 13106143 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Phenoxythiazole-4-carbaldehyde | HCID 13102642 | 57.1% |
Reaction Steps
19.1 g of manganese dioxide were added to a solution of 4.6 g of (2-phenoxy-4-thiazolyl)-methanol in 100 ml of benzene and the mixture was stirred at 60° C. for 3 hours and was filtered. The filtrate was evaporated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with an 8-2 methylene chloride-ethyl acetate mixture yielded 2.6 g of (2-phenoxy-4-thiazolyl)-methanal melting at 63° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04501894 |
|---|
| Source dataset | uspto-grants-1985_02 |
|---|
| ORD ID | ord-b556f6a83ccc4c45bcf7f3b861731ad0 |
|---|
| Source note | uspto-grants-1985_02 |
|---|