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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717843Generated: October 31, 2026

Ammonium cerium (IV) nitrate → 4-(3-Hydroxymethyl-[1,2,4]oxadiazol-5-ylmethyl)-benzoic acid ethyl ester

https://huagongshe.com/reaction/1717843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium cerium (IV) nitrateHCID 9869224—
Reactant4-[3-(4-Methoxy-phenoxymethyl)-[1,2,4]oxadiazol-5-ylmethyl]-benzoic acid ethyl esterHCID 66699565—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product4-(3-Hydroxymethyl-[1,2,4]oxadiazol-5-ylmethyl)-benzoic acid ethyl esterHCID 66699592528%

Reaction Steps

Add half of the ammonium cerium(IV) nitrate (285 mg, 0.52 mmol) to a solution of 4-[3-(4-methoxy-phenoxymethyl)-[1,2,4]oxadiazol-5-ylmethyl]-benzoic acid ethyl ester (193 mg, 0.52 mmol) in acetonitrile (9 mL) and water (2.3 mL) at room temperature. Stir the reaction mixture at room temperature for one hour and add the second half of the ammonium cerium(IV) nitrate (285 mg, 0.52 mmol). Stir at room temperature for an additional hour, dilute the reaction is with saturated aqueous sodium hydride CO3, stir for 5 minutes, dilute with water, and extract with ethyl acetate (3×). Wash the combined organic layers with brine, dry over MgSO4, and concentrate. Purify the residue by flash column chromatography using 50% ethyl acetate/hexane to give the title compound (720 mg, 81%). LC-MS (m/e): 263 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803938B2
Source datasetuspto-grants-2010_09
ORD IDord-c796efc1f5d8486fbaa17cfc0a9fe711
Source noteuspto-grants-2010_09