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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477321생성일: 2026년 10월 25일

(Phenylthio)acetic acid, cyclohexyl ester → 1-Ethyl 6-cyclohexyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioate

https://huagongshe.com/reaction/477321

반응식

참여 물질

역할이름HCID투입량
반응물(Phenylthio)acetic acid, cyclohexyl esterHCID 533051—
반응물N-(dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 86743575—
반응물Diethyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioateHCID 86743580—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물1-Ethyl 6-cyclohexyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioateHCID 86743586—

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 (13.7 g), a 1.6M solution (33.1 cc) of n-butyllithium in hexane and cyclohexyl (phenylthio)acetate (12 g) in tetrahydrofuran (150 cc). After purification by chromatography on a silica column with a mixture of cyclohexane and ethyl acetae (80:20 by volume) as eluent, 1-ethyl 6-cyclohexyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioate (9.7 g) is obtained, and is used in the crude state in the subsequent phases.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04886835
출처 데이터셋uspto-grants-1989_12
ORD IDord-1d8dd93c08b745c6a88ae596acca80ac
출처 메모uspto-grants-1989_12