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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327140Generated: October 30, 2026

Acetonitrile → 2-[6-(2-Chloro-4-methoxyphenoxy)hexyl]tetrazole

https://huagongshe.com/reaction/327140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantCesium carbonateHCID 10796—
Reactant2-{[6-(2-Chloro-4-methoxyphenoxy)hexyl]thio}-4,5-dihydrothiazol-4-oneHCID 18921835—
ReactantHCID 178418441HCID 178418441—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-[6-(2-Chloro-4-methoxyphenoxy)hexyl]tetrazoleHCID 18921909—

Reaction Steps

Stir overnight at room temperature 300 mg. of the iodide prepared in Examples 2 and 3, 3 ml. acetonitrile, 63 mg. 1-H-tetrazole and 274 mg. cesium carbonate in a reaction flask. Add an additional. 189 mg. 1-H-tetrazole and 100 mg. cesium carbonate,, let stir one week at room temperature. Work up the reaction mixture in methylene chloride with a water wash. Elute on a coarse silica column with methylene chloride then ethyl acetate/methylene chloride. Isolate two fractions of the title compound, the less polar fraction and the more polar fraction. One of the fractions is the 1-substituted tetrazole and the other fraction is the 2-substituted tetrazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05272167
Source datasetuspto-grants-1993_12
ORD IDord-7689ca9741ea470181bdc902611249f6
Source noteuspto-grants-1993_12