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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6896생성일: 2026년 10월 24일

Dimethylformamide → 5-Cyano-2-(3,4-Dichlorophenoxy)-Benzaldehyde

https://huagongshe.com/ko/reaction/6896

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물5-Bromo-2-(3,4-dichlorophenoxy)benzaldehydeHCID 12017030—
촉매Zinc cyanide (Zn(CN)2)HCID 11186—
촉매HCID 178418397HCID 178418397—
생성물5-Cyano-2-(3,4-Dichlorophenoxy)-BenzaldehydeHCID 12017050—

반응 단계

Under N2 in a flame-dried 3-neck round bottomed flask fitted with a reflux condenser and magnetic stirrer, a mixture of 5-bromo-2-(3,4-dichlorophenoxy)-benzaldehyde (3.0 g, 8.7 mmol), zinc (II) cyanide (1.5 g, 13 mmol) and tetrakis(triphenylphosphine)palladium (0) (1.5 g, 1.3 mmol) in anhydrous DMF (145 ml) was stirred at room temperature while degassing with N2 for 5 min. After heating at approximately 80° C. for 90 min., the reaction was judged complete by thin layer chromatography (50% CH2Cl2:hexanes) and was allowed to cool to room temperature. The reaction mixture was then diluted with water and ethyl acetate (EA) and stirred another 10 min. The water layer was separated, extracted twice with EA and combined with the original EA layer, and washed with an aqueous solution of Rochelle salt (potassium sodium tartrate tetrahydrate) followed by aqueous NaCl. The organic layer was dried with Na2SO4, filtered and concentrated in vacuo to an oil. The oil was flash chromatographed on a 15×5 cm column of silica gel, eluting with CH2Cl2:hexanes (1:1) to obtain the title product as a white solid, 1.5 g (60%), m.p. 122–126° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084165B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-422e54a7b8534818a58e13cc907fb18e
출처 메모uspto-grants-2006_08