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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19230생성일: 2026년 10월 23일

2,3-Difluorophenol → (E)-3-(2,3-difluoro-phenoxy)-but-2-enoic acid ethyl ester

https://huagongshe.com/ko/reaction/19230

반응식

참여 물질

역할이름HCID투입량
반응물2,3-DifluorophenolHCID 80879—
반응물3-Chloro-but-2-enoic acid ethyl esterHCID 282835—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물(E)-3-(2,3-difluoro-phenoxy)-but-2-enoic acid ethyl esterHCID 6689545666.1%

반응 조건

온도23 °C

반응 단계

Potassium t-butoxide (11.2 g, 0.100 mol) was added to a stirred solution of 2,3-difluoro-phenol (6.58 g, 0.051 mol) in tetrahydrofuran (30 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 7.50 g, 0.050 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-(2,3-difluoro-phenoxy)-but-2-enoic acid ethyl ester (8.01 g, 66%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741327B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c3fda18a84d748aea71152ef19409e57
출처 메모uspto-grants-2010_06