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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241913Generated: October 29, 2026

Benzoyl chloride, 3-nitro- → 3-(2,6-Dichlorophenyl)-5-(3-nitrophenyl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/1241913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3-nitro-HCID 8495—
ReactantSodium CarbonateHCID 10340—
Reactant2,6-dichloro-N'-hydroxybenzene-1-carboximidamideHCID 31956—
SolventPyridineHCID 1049—
Product3-(2,6-Dichlorophenyl)-5-(3-nitrophenyl)-1,2,4-oxadiazoleHCID 1135960842.1%

Reaction Steps

2,6-Dichlorobenzamidoxime (1.0 g) was dissolved in pyridine and m-nitrobenzoyl chloride (0.91 gm, 1.0 molar equivalent) was added. The solution was stirred at room temperature for 1 h under nitrogen, then heated at 90° C. for 4 h. The solution was cooled to room temperature, and poured into ice water. The pH of the solution was adjusted to approximately pH 10 with 2M aqueous sodium carbonate solution. The mixture was extracted with ether and the organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to dryness. The residue was dissolved in ethyl acetate. Addition of hexanes to the solution gave 3-(2,6-dichlorophenyl)-5-(3-nitrophenyl)-1,2,4-oxadiazole as a white solid (0.69 g). NMR (300 MHz, DMSO-d6): 8.52 (s, 1H), 8.38 (d, 1H), 8.18 (d, 1H), 7.78 (t, 1H), 7.57 ppm (m, 3H). LC-MS tr=38.2 min (Method W) MH++NA=359

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115642B2
Source datasetuspto-grants-2006_10
ORD IDord-0877faede32f48c0932167822bc029b5
Source noteuspto-grants-2006_10