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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19152생성일: 2026년 10월 23일

3-Cyanophenol → (E)-3-(3-cyano-phenoxy)-but-2-enoic acid methyl ester

https://huagongshe.com/ko/reaction/19152

반응식

참여 물질

역할이름HCID투입량
반응물3-CyanophenolHCID 13394—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물Methyl but-2-ynoateHCID 141019—
용매TetrahydrofuranHCID 8028—
생성물(E)-3-(3-cyano-phenoxy)-but-2-enoic acid methyl esterHCID 6689504776%

반응 단계

To a stirred mixture of 3-hydroxy-benzonitrile (3.30 g, 0.028 mol) and methyl-2-butynoate (5.40 g, 0.055 mol) in tetrahydrofuran (50 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (4.20 g, 0.028 mol) slowly. After addition was complete the mixture was stirred at reflux for 6 h. 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-(3-cyano-phenoxy)-but-2-enoic acid methyl ester as an oil (4.60 g, 76%) and used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741327B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-fb3e6c940794475996d3ab2a68d25e21
출처 메모uspto-grants-2010_06