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HRID 1584637作成日:2026年10月25日

Dimethylamine → 4-Dimethylamino-1-phenyl-3-butene-2-one

https://huagongshe.com/reaction/1584637

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物FormaldehydeHCID 712—
反応物m-Chloroperbenzoic acidHCID 70297—
反応物BenzylacetyleneHCID 575753—
反応物HCID 21225058HCID 21225058—
溶媒DichloromethaneHCID 6344—
生成物4-Dimethylamino-1-phenyl-3-butene-2-oneHCID 54570599—

反応条件

温度0 °C

反応手順

To an ice cold solution of 1-dimethylamino-4-phenyl-2-butyne (0.5 g; prepared by the Mannich reaction of 3-phenyl-1-propyne with formaldehyde and dimethylamine as per Mornet, et.al. Bull.Soc.Chim.Fr. 1974, 206) in dichloromethane (12 ml) was added in small portions 3-chloroperoxybenzoic acid (0.52 g). After the reaction was stirred at 0° C. for 20 minutes, the mixture was passed over twenty weight equivalents of basic alumina (Brockmann Grade I, 150 mesh) and the N-oxide was eluted using a solution of 10% methanol in dichloromethane. All fractions containing the desired amine N-oxide were combined and evaporated to near dryness in vacuo. The residue was treated successively three times with small portions of methanol (ca. 10 ml) followed by evaporation to near dryness, and the volume of the solution was adjusted to 25 mL by addition of methanol. The methanolic solution of the N-oxide was heated to reflux for approximately 4 hours and cooled. The solvent was evaporated to dryness in vacuo and the residue was chromatographed over silica gel (95:5 ethyl acetate-hexanes was used as the eluant) to give upon evaporation of the solvent in vacuo the desired product as an oil. MS(+ES) m/z: 190 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05932745
出典データセットuspto-grants-1999_08
ORD IDord-9b00bcf764d74c88946d8334b6a9109c
出典メモuspto-grants-1999_08