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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195144Generated: October 27, 2026

Sodium Iodide → 2-[4-[5-(3-Methylisoxazol-5-yl)pentoxy]phenyl]-1,3,4-oxadiazole

https://huagongshe.com/reaction/1195144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(1,3,4-Oxadiazol-2-yl)phenolHCID 714770—
Reactant5-(5-Bromopentyl)-3-methylisoxazoleHCID 13544046—
SolventAcetonitrileHCID 6342—
Product2-[4-[5-(3-Methylisoxazol-5-yl)pentoxy]phenyl]-1,3,4-oxadiazoleHCID 1483601540.6%

Reaction Steps

A mixture of 23.6 g 4-(1,3,4-oxadiazolyl)phenol (U.S. Pat. No. 4,218,458, Example XIX), 35 g 5-(5-bromopentyl)-3-methylisoxazole and 40 g milled potassium carbonate in 1.5 liters acetonitrile under nitrogen was heated to reflux. A catalytic amount of sodium iodide was added and refluxing continued for 4 hrs. The reaction mixture was filtered and concentrated to a solid residue. The latter was dissolved in ethyl acetate and the solution washed with water and saturated sodium chloride solution, dried over magnesium sulfate and concentrated in vacuo. The residue was recrystallized from triethylamine to give 18.5 g 3-methyl-5-{5-[4-(1,3,4-oxadiazol-2-yl)phenoxy]pentyl}isoxazole, white needles, m.p. 84°-86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110821
Source datasetuspto-grants-1992_05
ORD IDord-a9f531214ae74ab78c4cd4922d1e4ddc
Source noteuspto-grants-1992_05