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HRID 972680作成日:2026年10月25日

Cyanoacetamide → Piperidine

https://huagongshe.com/reaction/972680

反応式

関与物質

役割名称HCID仕込み量
反応物CyanoacetamideHCID 7898—
反応物Ethyl formateHCID 8025—
反応物4-DimethylaminoacetophenoneHCID 75037—
反応物SodiumHCID 5360545—
反応物Sodium MethoxideHCID 10942334—
反応物4-(Dimethylamino)-beta-oxobenzenepropanalHCID 12654798—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物PiperidineHCID 8082—
生成物6-[p-(Dimethylamino)phenyl]-1,2-dihydro-2-oxonicotinonitrileHCID 21404559—

反応手順

From a solution of the sodium salt of p-(dimethylamino)benzoylacetaldehyde in 400 ml. of water (prepared from 11.4 g. of sodium methoxide in 100 ml. of tetrahydrofuran and a solution of 29.3 g. of p-(dimethylamino)acetophenone [J.A.C.S. 73, 864 (1951)] and 13.3 g. of ethyl formate in 130 ml. of tetrahydrofuran), 18.5 g. of 2-cyanoacetamide and a solution consisting of 2.3 ml. of acetic acid, 5.2 ml. of water and 4.0 ml. of piperidine, there is obtained 6-[p-(dimethylamino)phenyl]-1,2-dihydro-2-oxonicotinonitrile; m.p. 280°-292° (dec.) after crystallization from aqueous dimethyl sulfoxide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04053470
出典データセットuspto-grants-1977_10
ORD IDord-47900b5405bc43558ffeb1bcdee85dfb
出典メモuspto-grants-1977_10