HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732132Generated: October 25, 2026
Benzonitrile, m-chloro- → 3-Bromo-5-(3-chlorophenyl)-1,2,4-oxadiazole
https://huagongshe.com/reaction/732132
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzonitrile, m-chloro- | HCID 13015 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-bromo-N-hydroxymethanecarbonimidoyl bromide | HCID 2763219 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Bromo-5-(3-chlorophenyl)-1,2,4-oxadiazole | HCID 67070903 | — |
Reaction Steps
Hydroxycarbonimidic dibromide (2.21 g, 10.89 mmol) was added portionwise over 1 h 20 min to a mixture of 3-chlorobenzonitrile (3.00 g, 21.29 mmol) and NaHCO3 (2.9 g, 34.87 mmol) in toluene (3 ml) at 90° C. Stirring was continued for 3 h and then the reaction mixture was cooled to r.t., diluted with EA and washed with water. The organic phase was dried and concentrated. A mixture of 3-chlorobenzonitrile and 3-bromo-5-(3-chlorophenyl)-1,2,4-oxadiazole was obtained after flash chromatography (hex/EA 10:1). 1.0 g of the mixture was dissolved in MeNH2 (4 ml, 8.5 M in EtOH) and heated in a microwave reactor for 30 min at 60° C. The volatiles were removed under reduced pressure and the residue was dissolved in water and extracted with CHCl3. The organic phase was dried and concentrated. Recrystallization from EA gave 137 mg of the title compound. 1H NMR: 3.00 (d, 3 H) 4.35 (bs, 1 H) 7.43 (t, 1 H) 7.50-7.55 (m, 1 H) 7.92 (d, 1 H) 8.03 (s, 1 H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07585881B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-1fcec38ba4fe4e71a2b688ccd8f544c4 |
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| Source note | uspto-grants-2009_09 |
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