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HRID 6896作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物5-Bromo-2-(3,4-dichlorophenoxy)benzaldehydeHCID 12017030—
触媒Zinc cyanide (Zn(CN)2)HCID 11186—
触媒HCID 178418397HCID 178418397—
生成物5-Cyano-2-(3,4-Dichlorophenoxy)-BenzaldehydeHCID 12017050—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084165B2
出典データセットuspto-grants-2006_08
ORD IDord-422e54a7b8534818a58e13cc907fb18e
出典メモuspto-grants-2006_08