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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461690Generated: October 30, 2026

Methylparaben → Benzoic acid, 4-[(tetrahydro-2H-pyran-2-yl)oxy]-, methyl ester

https://huagongshe.com/reaction/1461690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylparabenHCID 7456—
Reactant3,4-dihydro-2H-pyranHCID 8080—
CatalystSulfuric AcidHCID 1118—
ProductBenzoic acid, 4-[(tetrahydro-2H-pyran-2-yl)oxy]-, methyl esterHCID 11770459—

Reaction Steps

To a solution of 0.64 mL (2 mmol) of 1-(2-trimethylsiloxyethoxy)-1-trimethylsiloxy-2-methyl-lpropene, 0.55 mL of tetrabutylammonium biacetate (0.04 M in THF), and 0.06 mL of bis(dimethylamino)methylsilane in 40 mL of THF was added dropwise a solution of 20 g (72.5 mmol) of 4-tetrahydropyranyloxybenzyl methacrylate (purified by passing over a column of basic alumina in hexane solution, followed by evaporation of the hexane under reduced pressure) in 30 mL of THF. When the exothermic polymerization was finished, and the temperature had returned to room temperature, the reaction mixture was poured into methanol. Filtration gave 19 g of poly(4-tetrahydropyranyloxybenzyl methacrylate). GPD: Mn =9390, Mw =11,500, MwMn =1.23. DSC: Tg =62.3° C., with a decomposition endotherm at 250.5° C. TGA: rapid loss of 24.74% of weight at 248.1° C. The monomer was prepared from methyl 4-hydroxybenzoate by reaction with an excess of 3,4-dihydro-2H-pyran in the presence of sulfuric acid catalyst to give methyl 4-(2-tetrahydropyranyloxy)benzoate, which was then reduced with lithium aluminum hydride in THF solution to give 4-(2-tetrahydropyranyloxy)benzyl alcohol. Esterification with methacrylyl chloride and triethylamine in dichloromethane solution gave 4-tetrahydropyranyloxybenzyl methacrylate, m.p. 36° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05077174
Source datasetuspto-grants-1991_12
ORD IDord-bbf88f158adb46749b871e12441c9548
Source noteuspto-grants-1991_12