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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971593Generated: October 29, 2026

Hydrochloric Acid → 2-[(2-Methylprop-2-enoyl)oxy]benzoic acid

https://huagongshe.com/reaction/971593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant2-[(2-Methylprop-2-enoyl)oxy]benzoic acidHCID 198203—
CatalystPotassium PersulfateHCID 24412—
CatalystSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
Product2-[(2-Methylprop-2-enoyl)oxy]benzoic acidHCID 198203114%
ProductHCID 68543975HCID 68543975—

Reaction Steps

Sodium methacryloyloxybenzoate is prepared by dissolving 10 grams of methacryloyloxybenzoic acid in 150 ml of the aqueous solution containing 1.94 grams of sodium hydroxide. Twelve milliliters of 2 N NaOH solution is added in order to obtain a clear solution. To this solution maintained at 0°-5° C. and under nitrogen is added 0.15 grams of potassium persulfate in 7 ml of water, followed after one minute by 0.075 grams of sodium bisulfite in 5 ml of water. After the mixture is maintained at that temperature for 10 hours, it is allowed to rise to room temperature and stirred for an additional 16 hours. The reaction mixture is acidified with 100 ml of 20% by weight hydrochloric acid to precipitate the polymer. The polymer is filtered, washed with water, and then dried at 120° C./0.1 mm Hg to yield 5.7 grams of polymethacryloyloxybenzoic acid with an inherent viscosity of 1.46 (0.2%, 2 N NaOH, 25° ), and having a melting point of greater than 330° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04160755
Source datasetuspto-grants-1979_07
ORD IDord-8d77e31af5f146c391598dfe6caa6749
Source noteuspto-grants-1979_07