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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1033576생성일: 2026년 10월 27일

Cyanogen Bromide → 4,5-Dichloro-2-(3,4-dichlorophenyl)pyrrole-1,3-dicarbonitrile

https://huagongshe.com/reaction/1033576

반응식

참여 물질

역할이름HCID투입량
반응물Cyanogen BromideHCID 10476—
반응물4,5-dichloro-2-(3,4-dichlorophenyl)-1H-pyrrole-3-carbonitrileHCID 183555—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물4,5-Dichloro-2-(3,4-dichlorophenyl)pyrrole-1,3-dicarbonitrileHCID 1501015664.7%

반응 단계

Potassium t-butoxide (617 mg, 55 mmol) is added in portions to a solution of 3-cyano-4,5-dichloro 2-(3,4-dichlorophenyl)pyrrole (1.52 g, 5 mmol) in anhydrous THF (20 mL). After 30 minutes, a solution of cyanogen bromide (583 mg, 5.5 mmol) in THF (1 mL) is added. The reaction mixture is stored at room temperature overnight. The solvent is removed in a rotary evaporator. The residue is treated with water and extracted with ethyl acetate. The organic layer is washed with water and saturated sodium chloride and dried (MgSO4). Evaporation and crystallization of the residue from ethyl acetate gives while crystals (1.07 g); mp 250.5°-252.0° C.; IR (nujol) 2255, 2245 cm-1 (CN); 13C NMR (DMSO-d6) 102.7 (N--CN), 113.7 (3-CN); Mass spectrum 331.9 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05310938
출처 데이터셋uspto-grants-1994_05
ORD IDord-2a4f6d430cfc4aaf9f0e0611a7698463
출처 메모uspto-grants-1994_05