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HRID 1165571作成日:2026年10月24日

Pyridine → N-(3,4-Dichlorophenyl)-N-methyl-3-oxobutanamide

https://huagongshe.com/ja/reaction/1165571

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物DiketeneHCID 12661—
反応物3,4-Dichloro-N-methylanilineHCID 2800931—
溶媒TolueneHCID 1140—
生成物N-(3,4-Dichlorophenyl)-N-methyl-3-oxobutanamideHCID 13822492—

反応手順

Dissolved in toluene were 3.5 g (0.02 mole) of 3,4-dichloro-N-methylaniline and a catalytic amount of pyridine, followed by a dropwise addition of 1.9 g (0.022 mole) of diketene at 50° C. After completion of the the dropwise addition, the resultant mixture was heated under reflux for 3 hours. The reaction mixture was cooled, and its organic layer was then washed with water, water, a 10% aqueous solution of hydrochloric acid and a 5% aqueous solution of sodium hydrogencarbonate in order. The thus-washed organic solution was dried nd concentrated to obtain 3',4'-dichloro-N-methylacetoacetoanilide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04910315
出典データセットuspto-grants-1990_03
ORD IDord-7c0465aa519b451481169f1ecd662385
出典メモuspto-grants-1990_03