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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594233Generated: November 1, 2026

(3-(5-Methylthiazol-2-yl)phenyl)methanol → 3-(5-Methylthiazol-2-yl)benzaldehyde

https://huagongshe.com/reaction/594233

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-(5-Methylthiazol-2-yl)phenyl)methanolHCID 53273734—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product3-(5-Methylthiazol-2-yl)benzaldehydeHCID 53273723—

Reaction Steps

A solution of (3-(5-methylthiazol-2-yl)phenyl)methanol (210 mg; 1.02 mmol) in anh. DCM (8 ml) was treated with MnO2 (1.334 g; 15.34 mmol), and the resulting mixture was stirred at rt, under nitrogen, for 1.5 h. The resulting reaction mixture was then filtered over celite, and the separated solids were washed with DCM. The filtrate was concentrated to dryness under reduced pressure giving 3-(5-methylthiazol-2-yl)benzaldehyde as a colorless solid. LC-MS (conditions A): tR=0.72 min.; [M+H]+: 203.99 g/mol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-fe539833c462414f83844ae0aa2e46db
Source noteuspto-grants-2016_01