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HRID 1756816생성일: 2026년 10월 25일

Dimethylformamide → 2-Butyl-5-chloro-1H-imidazole-4-carbaldehyde

https://huagongshe.com/reaction/1756816

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium HydroxideHCID 14798—
반응물Phosphorus oxychlorideHCID 24813—
반응물2-butyl-3,5-dihydro-4H-imidazol-4-oneHCID 10909654—
용매ChlorobenzeneHCID 7964—
용매Ethyl AcetateHCID 8857—
생성물2-Butyl-5-chloro-1H-imidazole-4-carbaldehydeHCID 55176—
생성물2-butyl-3,5-dihydro-4H-imidazol-4-oneHCID 10909654—

반응 조건

온도100 °C

반응 단계

2-n-Butyl-2-imidazolin-5-one (9.81 g, 70 mmol) was added to a solution of phosphoroxychloride (26.83 g, 175 mmol) in chlorobenzene (50 ml) at room temperature. The orange suspension was heated to 100° C. within 5 minutes, and then N,N-dimethylformamide (12.79 g, 175 mmol) was added within 3 minutes. The black mixture was kept for 2 hours at 100° C., cooled to 40° C. and poured on water (84 ml). After addition of ethyl acetate (42 ml), the mixture was stirred for 15 minutes at 26° to 28° C. and then adjusted to pH 7 by addition of 30 percent sodium hydroxide solution (67 ml). The phases were separated, and the aqueous phase was extracted twice with 70 ml of ethyl acetate each. The combined organic phases were dried (MgSO4), filtered and concentrated by evaporation on a Rotavapor. The title compound was obtained in a yield of 8.31 g (64 percent) relative to the 2-n-butyl-2-imidazolin-5-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05442075
출처 데이터셋uspto-grants-1995_08
ORD IDord-d85c9d827bb94bcc9444f870b63b5a3a
출처 메모uspto-grants-1995_08