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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544443Generated: November 1, 2026

(2-Phenoxy-5-thiazolyl)-methanol → (2-Phenoxy-5-thiazolyl)-methanal

https://huagongshe.com/reaction/544443

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Phenoxy-5-thiazolyl)-methanolHCID 13106154—
CatalystHCID 178418406HCID 178418406—
SolventBenzeneHCID 241—
Product(2-Phenoxy-5-thiazolyl)-methanalHCID 1310615177.8%

Reaction Conditions

Temperature40 °C

Reaction Steps

40 g of manganese dioxide were added to a solution of 10 g of (2-phenoxy-5-thiazolyl)-methanol in 250 ml of benzene and the mixture was stirred at 40° C. for 5 hours and was filtered. The filtrate was evaporated to dryness and the residue was chromatographed over silica gel.Elution with a 7-3 methylene chloride-ethyl acetate mixture yielded 7.7 g of (2-phenoxy-5-thiazolyl)-methanal melting at 50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04450169
Source datasetuspto-grants-1984_05
ORD IDord-443ad994da514fe5b5c8f35a5e6df95e
Source noteuspto-grants-1984_05