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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229738Generated: October 26, 2026

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

https://huagongshe.com/reaction/2229738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantMethacrylic AcidHCID 4093—
ReactantEthylene glycol monoallyl etherHCID 8116—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventWaterHCID 962—
Product2-Propenoic acid, 2-methyl-, 2-(2-propen-1-yloxy)ethyl esterHCID 8560973%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a three-necked flask equipped with a stirrer, a thermometer, a ref lux condenser and a Dean-Stark apparatus were added methacrylic acid (137.7 g, 1.6 moles), ethyleneglycol monoallylether (80.7 g, 0.8 moles), p-toluenesulfonic acid (0.76 g, 4.0 mmole) and toluene (650 mL). The mixture was heated to 120° C. for 5 hours with exclusion of water. Another portion of p-toluenesulfonic acid (0.12 g) and the mixture was heated to 120° C. for 6 hours. The other portion of p-toluenesulfonic acid (0.1 g) was added and the mixture was heated to 120° C. for 9 hours. During the reaction, the consumption of methacrylic acid and ethyleneglycol monoallylether were monitored by liquid chromatography and the conversion reached 98%. The mixture was neutralized by addition of aq. NaHCO3 and the layers were separated. The aqueous layer was extracted with toluene and the combined organic layers were dried over CaCl2 and concentrated under reduced pressure. Distillation of the crude material (60° C. at 2 mmHg) yielded 2-allyloxyethyl methacrylate (98.7 g, 73%) shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420492B1
Source datasetuspto-grants-2002_07
ORD IDord-b43a434c13434d7c818a942bf5f119bb
Source noteuspto-grants-2002_07