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HRID 19132作成日:2026年10月25日
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/reaction/19132
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 反応物 | Methyl but-2-ynoate | HCID 141019 | — |
| 反応物 | 2-Fluoro-3-methoxyphenol | HCID 40151763 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (E)-3-(2-fluoro-3-methoxy-phenoxy)-but-2-enoic acid methyl ester | HCID 66895250 | 67.4% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07741327B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-37a162c02fd34c2c8bf49af0de73d76d |
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| 出典メモ | uspto-grants-2010_06 |
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