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HRID 1584637생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1584637

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물FormaldehydeHCID 712—
반응물m-Chloroperbenzoic acidHCID 70297—
반응물BenzylacetyleneHCID 575753—
반응물HCID 21225058HCID 21225058—
용매DichloromethaneHCID 6344—
생성물4-Dimethylamino-1-phenyl-3-butene-2-oneHCID 54570599—

반응 조건

온도0 °C

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05932745
출처 데이터셋uspto-grants-1999_08
ORD IDord-9b00bcf764d74c88946d8334b6a9109c
출처 메모uspto-grants-1999_08