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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1074039생성일: 2026년 10월 24일

Diisopropylamine → Ethyl 2-dimethylamino-5-ethoxycarbonyl-2,4-tridecadienoate

https://huagongshe.com/ko/reaction/1074039

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물Ethyl caprateHCID 8048—
반응물Ammonium ChlorideHCID 25517—
반응물N-(dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 86743575—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Ethyl 2-dimethylamino-5-ethoxycarbonyl-2,4-tridecadienoateHCID 5418096855.5%

반응 조건

온도-78 °C

반응 단계

Ethyl n-decanoate (10 g) is added in the course of 10 minutes at a temperature in the region of -78° C. to a stirred mixture of diisopropylamine (5.6 cc), a 1.6M solution (37.5 cc) of n-butyllithium in hexane and tetrahydrofuran (30 cc). Stirring is maintained for 30 minutes at the same temperature, N-(3-dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate (14.3 g) is then added and stirring is maintained for 3 hours at a temperature in the region of -78° C. After a gradual warming to approximately 20° C., ammonium chloride (4 g) dissolved in water (50 cc) is added to the reaction medium. Dichloromethane (200 cc) and water (100 cc) are added, and the organic phase is separated off after settling has taken place. The aqueous phase is washed with dichloromethane (2×50 cc). The organic phases are combined, dried over anhydrous magnesium sulphate, filtered and evaporated at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa). The residue is dissolved in a mixture (30 cc) of cyclohexane and ethyl acetate (60:40 by volume), and the solution obtained is poured onto silica (600 g) contained in a column 7 cm in diameter. Elution is performed with a mixture of cyclohexane and ethyl acetate (60:40 by volume), and the eluate is concentrated to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa). Ethyl 2-dimethylamino-5-ethoxycarbonyl-2,4-tridecadienoate (9.8 g) is thereby obtained, and is used in the crude state in the subsequent syntheses.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04971979
출처 데이터셋uspto-grants-1990_11
ORD IDord-a3d1e68505bd48b383e20fec03bb0674
출처 메모uspto-grants-1990_11