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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 732132생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/732132

반응식

참여 물질

역할이름HCID투입량
반응물Benzonitrile, m-chloro-HCID 13015—
반응물Sodium BicarbonateHCID 516892—
반응물1-bromo-N-hydroxymethanecarbonimidoyl bromideHCID 2763219—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물3-Bromo-5-(3-chlorophenyl)-1,2,4-oxadiazoleHCID 67070903—

반응 단계

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)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07585881B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-1fcec38ba4fe4e71a2b688ccd8f544c4
출처 메모uspto-grants-2009_09