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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603175Generated: October 26, 2026

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

https://huagongshe.com/reaction/1603175

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 reflux 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 numberUS05986014
Source datasetuspto-grants-1999_11
ORD IDord-c8f8bbbccf144cedbb0ffef76f2f44b6
Source noteuspto-grants-1999_11