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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258315Generated: October 26, 2026

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

https://huagongshe.com/reaction/1258315

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 numberUS08466148B2
Source datasetuspto-grants-2013_06
ORD IDord-ee07ba6d49ea4b1ea04ecb762b4b34f2
Source noteuspto-grants-2013_06