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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477343생성일: 2026년 10월 24일

Dimethylammonium tetrafluoroborate → Ethyl 2-dimethylamino-6-(4-biphenylyl)-5-methylthio-6-oxo-2,4-hexadienoate

https://huagongshe.com/ko/reaction/477343

반응식

참여 물질

역할이름HCID투입량
반응물Dimethylammonium tetrafluoroborateHCID 140161—
반응물Sodium ethoxideHCID 2723922—
반응물Ethyl 6-phenyl-6-oxo-5-methylthio-2-dimethylamino2,4-hexadienoateHCID 44325574—
용매EthanolHCID 702—
생성물Ethyl 2-dimethylamino-6-(4-biphenylyl)-5-methylthio-6-oxo-2,4-hexadienoateHCID 54170142—

반응 단계

The procedure is as in Example 4 for the preparation of ethyl 6-phenyl-6-oxo-5-methylthio-2dimethylamino-2,4-hexadienoate, starting with N-(3-dimethylamino)-3-ethoxycarbonylpropenyldiene)-N-methylmethanaminium tetrafluoroborate (6 g), a 2M ethanolic solution of sodium ethylate (10.5 cc) and α-methylthio-4-phenylacetophenone (5.1 g) in ethanol (150 cc). After purification by chromatography on a silica column with a mixture of cyclohexane and ethyl acetate (50:50 by volume) as eluent, ethyl 2-dimethylamino-6-(4-biphenylyl)-5-methylthio-6-oxo-2,4-hexadienoate (2.8 g) is obtained in the form of an orange-coloured oil, and is used in the crude state in the subsequent syntheses.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04886835
출처 데이터셋uspto-grants-1989_12
ORD IDord-71bc1b8e1b25490a8350181c257f760a
출처 메모uspto-grants-1989_12