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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31411Generated: October 25, 2026

Triethyl orthoacetate → 2-(4-Iodophenyl)-5-methyl-[1,3,4]oxadiazole

https://huagongshe.com/reaction/31411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl orthoacetateHCID 66221—
Reactant4-IodobenzenecarbohydrazideHCID 306104—
Product2-(4-Iodophenyl)-5-methyl-[1,3,4]oxadiazoleHCID 676569—

Reaction Conditions

Temperature130 °C

Reaction Steps

Triethyl orthoacetate (10 ml) was added to 4-iodo-benzoic acid hydrazide (Intermediate 14) (0.55 g, 2.1 mmol) and heated under nitrogen at 130° C. for 3 hours. The triethyl orthoacetate was removed in vacuo and the residue partitioned between ethyl acetate (30 ml) and water (30 ml). The organic layer was washed with water (50 ml), brine (50 ml), dried over magnesium sulfate filtered and the solvent removed in vacuo. The residue was purified by silica SPE cartridge (10 g) eluting with 20:1 cyclohexane/ethyl acetate v:v to 5:1 cyclohexane/ethyl acetate v:v. The desired product was obtained as a white solid (0.31 g, 1.1 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425555B2
Source datasetuspto-grants-2008_09
ORD IDord-83ed388e738c4ac3a3d041d293b05383
Source noteuspto-grants-2008_09