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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 반응물 | Methyl but-2-ynoate | HCID 141019 | — |
| 반응물 | 2-Fluoro-3-methoxyphenol | HCID 40151763 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (E)-3-(2-fluoro-3-methoxy-phenoxy)-but-2-enoic acid methyl ester | HCID 66895250 | 67.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07741327B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-37a162c02fd34c2c8bf49af0de73d76d |
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| 출처 메모 | uspto-grants-2010_06 |
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