HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570340Generated: October 29, 2026
Dimethylformamide → 5-Chloro-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole
https://huagongshe.com/reaction/570340
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazol-5(4H)-one | HCID 136334039 | — |
| Product | 5-Chloro-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole | HCID 71281352 | — |
Reaction Steps
To a solution of 3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazol-5(4H)-one (106) (12 g, 54.26 mmol) in POCl3 (120 mL) was added N,N-dimethylformamide (12 mL). The resulted solution was heated to reflux for 72 hours then concentrated under vacuum. The residue was dissolved in water (250 mL) and extracted with ethyl acetate (3×250 mL). The combined organic layers were washed with brine (3×250 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified by flash chromatography (PE/EA=10:1) to afford 5-chloro-3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazole (107) as a white solid. 1H NMR (300 MHz, CDCl3) δ 8.64 (dd, J=1.5, 8.4 Hz, 1H), 8.18 (dd, J=1.5, 7.8 Hz, 1H), 7.56 (d, J=8.1 Hz, 1H), 2.70 (s, 3H). MS m/z 240.7 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023839B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-e1bbcbe0925c42a78d187ad562962f9a |
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| Source note | uspto-grants-2015_05 |
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