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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655434Generated: October 25, 2026

Ethanol → Ethyl 2,1,3-benzoxadiazole-5-carboxylate

https://huagongshe.com/reaction/655434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
Reactant2,1,3-Benzoxadiazole-5-carbonitrileHCID 2735452—
ProductEthyl 2,1,3-benzoxadiazole-5-carboxylateHCID 273636875%

Reaction Steps

To a solution of benzo[c][1,2,5]oxadiazole-5-carbonitrile (700 mg, 1.33 mol) in EtOH (100 mL) was added H2SO4 (20 mL) and the reaction mixture was refluxed for 14 h. The reaction was concentrated in vacuo and the residue was diluted with water (50 mL), and extracted with DCM (2×100 mL). The combined organic layers were dried over magnesium sulfate, filtered, and then concentrated in vacuo to afford ethyl benzo[c][1,2,5]oxadiazole-5-carboxylate (0.7 g, 75%) as a yellow, sticky solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071595B2
Source datasetuspto-grants-2011_12
ORD IDord-0851decbf47b413ab11b58da53d64004
Source noteuspto-grants-2011_12