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HRID 19206생성일: 2026년 10월 24일

2-Isopropoxyphenol → (E)-3-(2-isopropoxy-phenoxy)-but-2-enoic acid ethyl ester

https://huagongshe.com/ko/reaction/19206

반응식

참여 물질

역할이름HCID투입량
반응물2-IsopropoxyphenolHCID 20949—
반응물3-Chloro-but-2-enoic acid ethyl esterHCID 282835—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물(E)-3-(2-isopropoxy-phenoxy)-but-2-enoic acid ethyl esterHCID 6689453165%

반응 조건

온도23 °C

반응 단계

Potassium t-butoxide (7.36 g, 0.066 mol) was added to a stirred solution of 2-isopropoxy-phenol (5.00 g, 0.033 mol) in tetrahydrofuran (35 mL) at 23° C. under nitrogen and the reaction mixture was heated to reflux for 0.75 h. The reaction mixture was cooled to 23° C. and a solution of 3-chloro-but-2-enoic acid ethyl ester (prepared as in Example 191, 4.86 g, 0.033 mol) in tetrahydrofuran (40 mL) was added to the reaction mixture. The reaction mixture was refluxed for an additional 3 h. After this time, the mixture was concentrated in vacuo and the residue was diluted with water and extracted with diethyl ether. The organic layer was then washed with 5% aqueous sodium hydroxide solution followed by a saturated aqueous sodium chloride solution, dried over sodium sulfate and concentrated in vacuo to afford (E)-3-(2-isopropoxy-phenoxy)-but-2-enoic acid ethyl ester (5.60 g, 65%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741327B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6415b3daebf74f38bf959cf212dac43f
출처 메모uspto-grants-2010_06