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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19132생성일: 2026년 10월 24일

1,8-Diazabicyclo(5.4.0)undec-7-ene → (E)-3-(2-fluoro-3-methoxy-phenoxy)-but-2-enoic acid methyl ester

https://huagongshe.com/ko/reaction/19132

반응식

참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물Methyl but-2-ynoateHCID 141019—
반응물2-Fluoro-3-methoxyphenolHCID 40151763—
용매TetrahydrofuranHCID 8028—
생성물(E)-3-(2-fluoro-3-methoxy-phenoxy)-but-2-enoic acid methyl esterHCID 6689525067.4%

반응 단계

To a stirred mixture of 2-fluoro-3-methoxy-phenol (3.88 g, 0.027 mol) and methyl-2-butynoate (5.97 g, 0.061 mol) in tetrahydrofuran (30 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (4.64 g, 0.030 mol) slowly. After addition was complete the mixture was stirred at reflux overnight. Upon completion of the reaction the tetrahydrofuran was removed in vacuo and the residue was diluted in diethyl ether and washed first with 1N aqueous hydrochloric acid, then 10% aqueous sodium hydroxide solution, a saturated sodium chloride solution and dried over magnesium sulfate. The mixture was filtered and evaporated and the residue dried under high vacuum which afforded (E)-3-(2-fluoro-3-methoxy-phenoxy)-but-2-enoic acid methyl ester (4.37 g, 63%) as a colorless oil and used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741327B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-37a162c02fd34c2c8bf49af0de73d76d
출처 메모uspto-grants-2010_06