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HRID 1247543생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1247543

반응식

참여 물질

역할이름HCID투입량
반응물Methacrylic AcidHCID 4093—
반응물Ethylene glycol monoallyl etherHCID 8116—
반응물Sodium BicarbonateHCID 516892—
촉매p-Toluenesulfonic acidHCID 6101—
용매TolueneHCID 1140—
생성물2-Propenoic acid, 2-methyl-, 2-(2-propen-1-yloxy)ethyl esterHCID 8560973%

반응 단계

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

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07129294B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-e71e9543e701480dbad539a47b10e2b4
출처 메모uspto-grants-2006_10