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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308029Generated: October 31, 2026

Sulfuric Acid → 1-ethylcyclohexyl methacrylate

https://huagongshe.com/reaction/2308029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantMethacrylic AcidHCID 4093—
ReactantSodium HydroxideHCID 14798—
Reactant1-EthylcyclohexeneHCID 73937—
SolventTolueneHCID 1140—
Product1-ethylcyclohexyl methacrylateHCID 1136759169.9%

Reaction Conditions

Temperature30 °C

Reaction Steps

A 500 ml flask was flushed with nitrogen to displace the air with nitrogen, and was charged with 43.0 g (0.5 mol) of methacrylic acid, 0.5 g (5 mmol) of sulfuric acid and 100 g of toluene. Separately 110.2 g (1.0 mol) of 1-ethylcyclohexene, prepared by the same procedures as described in Reference Example 3, was dissolved in 100 g of toluene. The obtained solution of 1-ethylcyclohexene in toluene was dropwise added to the content in the flask over a period of about 3 hours, while the content was maintained at a reaction temperature of about 30° C. Then the content was stirred for 15 hours at the same temperature. After completion of the reaction, the residual catalyst was neutralized by adding 40.0 g (50 mmol) of a 5% aqueous sodium hydroxide solution, and the neutralized liquid was washed with an aqueous saturated sodium chloride solution. The thus-obtained organic phase was subjected to column chromatography, and further, analyzed by NMR and mass spectrometry. Thus, 68.6 g (yield: 69.9%) of the object 1-ethylcyclohexyl methacrylate was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06833462B2
Source datasetuspto-grants-2004_12
ORD IDord-4cf8a06265904f65b5aaa52426c8fc81
Source noteuspto-grants-2004_12