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HRID 21890作成日:2026年10月25日

Dimethylformamide → 2-(1-Methylbutyloxy)-3-dimethylaminoacrolein

https://huagongshe.com/reaction/21890

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物2-(4-Methylbutyloxy)acetaldehyde diethylacetalHCID 19930625—
溶媒1,1-DichloroethaneHCID 6365—
生成物2-(1-Methylbutyloxy)-3-dimethylaminoacroleinHCID 53907798—

反応条件

温度5 °C

反応手順

A solution prepared by adding 30 g of dried N,N-dimethylformamide to dried dichloroethane was cooled to 5° C. or lower, After a solution containing 63 g of phosphorus oxychlorate dissolved in dichloroethane was added to the cooled solution dropwise, the mixture was stirred for 30 minutes at 5° C. or lower. Subsequently, to the reaction solution was added a dichloroethane solution of the compound (54), and the resulting mixture was stirred for 30 minutes at room temperature and then for one hour at 70° C. After the reaction solution was cooled to room temperature, the reaction solution was poured into ice water and was then made basic by addition of potassium carbonate. The reaction solution was then concentrated under reduced pressure. The concentrate was warmed and stirred, and was then extracted with ethyl acetate. After the extract was dried over magnesium sulfate, the solvent used was distilled out. The residue was distilled under reduced pressure to obtain 2-(1-methylbutyloxy)-3-dimethylaminoacrolein (55) (boiling point: 150° to 155° C./5 mmHg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05425897
出典データセットuspto-grants-1995_06
ORD IDord-85e7fbe5696e42ed975adf7ba2536fc2
出典メモuspto-grants-1995_06