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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468967Generated: November 1, 2026

Triethyl phosphite → 5-Bromo-6-chlorobenzo[c][1,2,5]oxadiazole

https://huagongshe.com/reaction/1468967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphiteHCID 31215—
Reactant6-Bromo-5-chlorobenzo[c][1,2,5]oxadiazole 1-oxideHCID 67465069—
SolventEthanolHCID 702—
Product5-Bromo-6-chlorobenzo[c][1,2,5]oxadiazoleHCID 6746846879%

Reaction Steps

6-Bromo-5-chlorobenzo[c][1,2,5]oxadiazole 1-oxide (4.8 g, 19 mmol) was taken up 150 ml ethanol, heated to reflux, treated with triethyl phosphite (8.8 g, 53 mmol) and heated for 3.5 h. After cooling, the volatiles were removed by rotary evaporation, the residue was taken up in 100 mL dichloromethane and stirred with 50 mL bleach solution for 30 min. The organic phase was washed with 20 mL saturated NaCl, dried (Na2SO4) and evaporated. The crude material was purified by flash chromatography with a 0-30% ethyl acetate-hexane gradient to give the title compound as an orange solid (3.5 g, 79%): mp 68-69° C.; 1H NMR (400 MHz, CDCl3) δ 8.30 (s, 1H), 8.05 (s, 1H); EIMS m/z 232.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006250B2
Source datasetuspto-grants-2015_04
ORD IDord-dd4ba333b7224aa28c5526d6bbc0aadb
Source noteuspto-grants-2015_04