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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12591생성일: 2026년 10월 23일

Triethyl phosphonoacetate → (E)-(R)-4-tert-butoxycarbonylamino-6-(4-heptyloxy-phenyl)-4-methyl-hex-2-enoic acid ethyl ester

https://huagongshe.com/ko/reaction/12591

반응식

참여 물질

역할이름HCID투입량
반응물Triethyl phosphonoacetateHCID 13345—
반응물Sodium BicarbonateHCID 516892—
반응물[(R)-1-Formyl-3-(4-heptyloxy-phenyl)-1-methyl-propyl]-carbamic acid tert-butyl esterHCID 59339517—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(E)-(R)-4-tert-butoxycarbonylamino-6-(4-heptyloxy-phenyl)-4-methyl-hex-2-enoic acid ethyl esterHCID 58897683—

반응 조건

온도-78 °C

반응 단계

To a stirred solution of (diethoxy-phosphoryl)-acetic acid ethyl ester (429 mg, 1.92 mMol) in dry THF (7 ml) is added n-butyllithium (0.66 ml, 2.5M in hexane, 1.66 mMol) at −78° C. The mixture was stirred at −78° C. for 1 hour. After that time, a solution of [(R)-1-formyl-3-(4-heptyloxy-phenyl)-1-methyl-propyl]-carbamic acid tert-butyl ester (500 mg, 1.28 mMol) in THF (4 ml) is added and stirring is continued at −78° C. for 1.5 hours. The mixture is allowed to warm to RT and then stirred at RT for 2 hours. The reaction mixture is then poured onto a biphasic mixture of AcOEt and NaHCO3 (saturated aqueous solution) and the aqueous phase is extracted twice with AcOEt. The combined organic layers are dried (Na2SO4) and concentrated under reduced pressure. Column chromatography eluting with 4% AcOEt in toluene gives the title compound as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728020B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e219271ff5654914b84b2a1a70a9aa35
출처 메모uspto-grants-2010_06