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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594212Generated: November 2, 2026

(2-Phenoxythiazol-4-yl)methanol → 2-Phenoxythiazole-4-carbaldehyde

https://huagongshe.com/reaction/594212

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Phenoxythiazol-4-yl)methanolHCID 13106143—
CatalystManganese dioxideHCID 14801—
Solvent1,2-DichloroethaneHCID 11—
Product2-Phenoxythiazole-4-carbaldehydeHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-c60ea672fb81455492d4d2b0a0a88ed2
Source noteuspto-grants-2016_01