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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340816Generated: October 30, 2026

Hydroquinone → HCID 14401402, compound

https://huagongshe.com/reaction/340816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroquinoneHCID 785—
ReactantMethacrylic AcidHCID 4093—
ReactantUndec-1-en-1-olHCID 44135745—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventBenzeneHCID 241—
ProductHCID 14401402HCID 1440140251.2%

Reaction Steps

Monomer synthesis. In a 3 neck round bottom flask, methacrylic acid (51.4 g, 0.515 mol) and benzene (60 ml) were combined. P-TSA (0.90 g, 2.6 mmol), hydroquinone (1.56 g, 13.6 mmol) and undecene-1-ol (25.8 g, 0.150 mol) were added into the flask and a Dean Stark adapter was attached. The reaction was heated at reflux overnight. The benzene was removed from the solution by rotary evaporation at reduced pressure and ether (200 ml) was added. NaHCO3 (50 g) was added to the ether solution to remove any excess methacrylic acid. The product was decanted from the NaHCO3 and washed with H2O (200 ml) 3 times, with 5% by weight NaHCO3 (200 ml) solution 3 times, and again with H2O (200 ml) 3 times. The product was dried over MgSO4 and the ether was removed by rotary evaporation. The product was distilled at 110° C. at 150 mTorr to yield 18.3 g (51% yield) of undec-10-enyl methacrylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895667B2
Source datasetuspto-grants-2014_11
ORD IDord-8ceec9c534694023b63de58622db08e0
Source noteuspto-grants-2014_11