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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4354Generated: October 25, 2026

m-Chloroperbenzoic acid → 4-[2-(Phenylmethyl)-4-thiazolyl]pyridine-1-oxide

https://huagongshe.com/reaction/4354

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-(2-Benzyl-1,3-thiazol-4-yl)pyridineHCID 14096952—
SolventDichloromethaneHCID 6344—
Product4-[2-(Phenylmethyl)-4-thiazolyl]pyridine-1-oxideHCID 1423105495%

Reaction Steps

To a suspension of m-chloroperbenzoic acid (14.5 g) in dry methylene chloride (150 mL) was added a solution of 2-benzyl-4-(4-pyridyl)thiazole (15.1 g, 0.06 mol) in methylene chloride (125 mL) over thirty minutes. The mixture was allowed to stir overnight at room temperature then an additional portion of m-chloroperbenzoic acid (3.00 g) was added. After an additional six hours of stirring the mixture was extracted with saturated sodium bicarbonate (3×100 mL). The organic layer was dried over sodium sulfate, and concentrated to a total volume of 75 mL. Dilution with ether (200 mL) afforded 4-[2-(phenylmethyl)-4-thiazolyl]pyridine-1-oxide (15.3 g, 95%). Recrystallization from ethanol/ether afforded an analytical sample. mp. 170°-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04725606
Source datasetuspto-grants-1988_02
ORD IDord-c6e1cc3c94154c00aca4659516630175
Source noteuspto-grants-1988_02