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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544444Generated: November 2, 2026

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

https://huagongshe.com/reaction/544444

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Phenoxythiazol-4-yl)methanolHCID 13106143—
CatalystHCID 178418406HCID 178418406—
SolventBenzeneHCID 241—
Product2-Phenoxythiazole-4-carbaldehydeHCID 1310264257.1%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04450169
Source datasetuspto-grants-1984_05
ORD IDord-80b1614af7264a85beff8f63b9b2c06c
Source noteuspto-grants-1984_05