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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl chloride, 3-nitro- | HCID 8495 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,6-dichloro-N'-hydroxybenzene-1-carboximidamide | HCID 31956 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-(2,6-Dichlorophenyl)-5-(3-nitrophenyl)-1,2,4-oxadiazole | HCID 11359608 | 42.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115642B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-0877faede32f48c0932167822bc029b5 |
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| Source note | uspto-grants-2006_10 |
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