戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 732132作成日:2026年10月27日

Benzonitrile, m-chloro- → 3-Bromo-5-(3-chlorophenyl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/732132

反応式

関与物質

役割名称HCID仕込み量
反応物Benzonitrile, m-chloro-HCID 13015—
反応物Sodium BicarbonateHCID 516892—
反応物1-bromo-N-hydroxymethanecarbonimidoyl bromideHCID 2763219—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物3-Bromo-5-(3-chlorophenyl)-1,2,4-oxadiazoleHCID 67070903—

反応手順

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)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07585881B2
出典データセットuspto-grants-2009_09
ORD IDord-1fcec38ba4fe4e71a2b688ccd8f544c4
出典メモuspto-grants-2009_09