戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 19152作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物3-CyanophenolHCID 13394—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物Methyl but-2-ynoateHCID 141019—
溶媒TetrahydrofuranHCID 8028—
生成物(E)-3-(3-cyano-phenoxy)-but-2-enoic acid methyl esterHCID 6689504776%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741327B2
出典データセットuspto-grants-2010_06
ORD IDord-fb3e6c940794475996d3ab2a68d25e21
出典メモuspto-grants-2010_06