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HRID 1247543作成日:2026年10月26日

Methacrylic Acid → 2-Propenoic acid, 2-methyl-, 2-(2-propen-1-yloxy)ethyl ester

https://huagongshe.com/reaction/1247543

反応式

関与物質

役割名称HCID仕込み量
反応物Methacrylic AcidHCID 4093—
反応物Ethylene glycol monoallyl etherHCID 8116—
反応物Sodium BicarbonateHCID 516892—
触媒p-Toluenesulfonic acidHCID 6101—
溶媒TolueneHCID 1140—
生成物2-Propenoic acid, 2-methyl-, 2-(2-propen-1-yloxy)ethyl esterHCID 8560973%

反応手順

A three-necked flask equipped with stirrer, thermometer, reflux condenser and Dean-Stark trap is charged with methacrylic acid (137.7 g, 1.6 mol), ethylene glycol monoallyl ether (80.7 g, 0.8 mol), p-toluenesulfonic acid (0.76 g, 4.0 mmol) and toluene (650 mL). After allowing the reaction to proceed at 120° C. for 5 hours, 0.12 g of p-toluenesulfonic acid is added, and the reaction is further allowed to proceed at the same temperature for 6 hours. Then, 0.1 g of p-toluenesulfonic acid is added, and the reaction is further allowed to proceed at the same temperature for 9 hours, whereupon the reaction is completed. During the whole reaction period, methacrylic acid and ethylene glycol monoallyl ether are monitored with liquid chromatography. The final conversion amounted to 98%. The reaction mixture is neutralized by adding an aqueous solution of NaHCO3 and allowed to separate into two layers. The aqueous layer is extracted once with toluene. The combined organic layer is dried over CaCl2 and the volatile matter is distilled off under reduced pressure. The crude product is distilled under reduced pressure (60° C., 2 mmHg) to give 98.7 g (73% yield) of 2-allyloxyethyl methacrylate shown below. H2C═C(CH3)CO2(CH2)2OCH2CH═CH2

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07129294B2
出典データセットuspto-grants-2006_10
ORD IDord-e71e9543e701480dbad539a47b10e2b4
出典メモuspto-grants-2006_10