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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290771Generated: October 29, 2026

Methanol → 3-Carboxymethyl-5-(3-fluoro-4-phenyl-alpha-methylbenzyl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/2290771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
Reactant3-Cyanomethyl-5-(3-fluoro-4-phenyl-alpha-methylbenzyl)-1,2,4-oxadiazoleHCID 13690968—
SolventWaterHCID 962—
Product3-Carboxymethyl-5-(3-fluoro-4-phenyl-alpha-methylbenzyl)-1,2,4-oxadiazoleHCID 13690969—

Reaction Steps

To a solution of 1.4 g of 3-cyanomethyl-5-(3-fluoro-4-phenyl-α-methylbenzyl)-1,2,4-oxadiazole obtained in Example 38 in 50 ml of methanol was added a solution of 2.56 g of potassium hydroxide in 23 g of water. After stirring under reflux for 4 hours, the reaction mixture was cooled, diluted with water and extracted with chloroform. The organic phase was washed with water, dried over sodium sulfate and evaporated. The residue was chromatographed over silica gel using chloroformmethanol (20:1, v/v) to give 1.35 g of 3-carboxymethyl-5-(3-fluoro-4-phenyl-α-methylbenzyl)-1,2,4-oxadiazole as an oil. It was crystallized from diisopropyl ether to give colorless fine needles, m.p. 100.5°-101.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04618617
Source datasetuspto-grants-1986_10
ORD IDord-db7455bdb2cf4748826b194a4ae5ae2a
Source noteuspto-grants-1986_10