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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205543Generated: November 1, 2026

4-Fluorobenzohydrazide → HCID 17951329, compound

https://huagongshe.com/reaction/2205543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzohydrazideHCID 9972—
ReactantEthyl orthoformateHCID 31214—
ProductHCID 17951329HCID 1795132957%

Reaction Steps

A stirred solution of 4-fluorobenzohydrazide (4.2 g, 27.2 mmol) in triethylorthoformate (27 mL) was heated at 140° C. for 5 h. The reaction was evaporated under reduced pressure. The crude was purified by silica gel column chromatography (100-200 mesh; using 12% ethyl acetate in hexane) to afford 2-(4-fluorophenyl)-1,3,4-oxadiazole [Polshettiwar, Tetrahedron Letters, 49:879-883 (2008)] as off-white solid (2.5 g, 57% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.46 (s, 1H), 8.08 (dd, 2H), 7.19 (dd, 2H); LC-MS m/z calculated for [M+H]+165.04. found 165.00.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371316B2
Source datasetuspto-grants-2016_06
ORD IDord-cf8d9a7e569149e98fc7c7f04082f4fa
Source noteuspto-grants-2016_06