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HRID 19279作成日:2026年10月26日

M-Cresol → (E)-3-m-tolyloxy-but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/19279

反応式

関与物質

役割名称HCID仕込み量
反応物M-CresolHCID 342—
反応物3-Chloro-but-2-enoic acid ethyl esterHCID 282835—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物(E)-3-m-tolyloxy-but-2-enoic acid ethyl esterHCID 1224119763.3%

反応条件

温度23 °C

反応手順

Potassium t-butoxide (10.4 g, 0.092 mol) was added to a stirred solution of 3-methyl-phenol (5.00 g, 0.046 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, 6.85 g, 0.046 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-m-tolyloxy-but-2-enoic acid ethyl ester (6.41 g, 63%) as a yellow oil.

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-933c811e9bc548a696a80249e8acda47
出典メモuspto-grants-2010_06