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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474348Generated: October 31, 2026

Ethanol → 5-Ethenyl-2,1,3-benzoxadiazole

https://huagongshe.com/reaction/1474348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant5-Bromo-2,1,3-benzoxadiazoleHCID 2776298—
Product5-Ethenyl-2,1,3-benzoxadiazoleHCID 59568720—

Reaction Steps

5-Bromo-2,1,3-benzoxadiazole (5.5 g, 27.6 mmol)), potassium vinylfluoroborate (7.40 g, 55.3 mmol), and PdCl2(dppf)-CH2Cl2Adduct (1.088 g, 1.332 mmol) were suspended in ethanol (75 ml) then added TEA (7.70 ml, 55.3 mmol). The reaction mixture was then degassed and heated to reflux for 3 hrs. The reaction was diluted with ethyl acetate and washed with brine. The organic layer was dried over Na2SO4, filtered and evaporated to dryness. The residue was purified through a 330 g ISCO Redi-Sep silica gel plug and eluted with 20% ETOAc/hexane to yield 5-ethenyl-2,1,3-benzoxadiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018211B2
Source datasetuspto-grants-2015_04
ORD IDord-c1491ce5133c4945bbfd30ba659086c1
Source noteuspto-grants-2015_04