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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477348생성일: 2026년 10월 24일

alpha-Naphthaleneacetic acid, ethyl ester → Diethyl 2-dimethylamino-5-(1-naphthyl)-2,4-hexadienedioate

https://huagongshe.com/ko/reaction/477348

반응식

참여 물질

역할이름HCID투입량
반응물alpha-Naphthaleneacetic acid, ethyl esterHCID 62428—
반응물Sodium ethoxideHCID 2723922—
반응물N-(dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 86743575—
반응물Diethyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioateHCID 86743580—
용매EthanolHCID 702—
생성물Diethyl 2-dimethylamino-5-(1-naphthyl)-2,4-hexadienedioateHCID 5399413917.1%

반응 단계

The procedure is as in Example 2 for the preparation of diethyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioate, starting with N-(3-dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate (10 g), a 2M ethanolic solution of sodium ethylate (26 cc) and ethyl 2-(1-naphthyl)acetate (7.5 g) in ethanol (100 cc). After purification by chromatography on a silica column with a mixture of cyclohexane and ethyl acetate (80:20 by volume), diethyl 2-dimethylamino-5-(1-naphthyl)-2,4-hexadienedioate (2.2 g) is obtained in the form of a yellow 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-680d84392e4040ff89533067cd470af4
출처 메모uspto-grants-1989_12