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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42734Generated: October 25, 2026

Potassium Carbonate → Acrylic acid 4-[3-(4-benzoyl-phenoxy)-2-hydroxy-propoxy]butyl ester

https://huagongshe.com/reaction/42734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-HydroxybenzophenoneHCID 14347—
Reactant4-Hydroxybutylacrylate glycidyletherHCID 22323150—
SolventAcetonitrileHCID 6342—
ProductAcrylic acid 4-[3-(4-benzoyl-phenoxy)-2-hydroxy-propoxy]butyl esterHCID 58325536101.1%

Reaction Steps

A reaction mixture containing 4-hydroxybenzophenone (14.9 g, 75 mmol), acetonitrile (40 mL), potassium carbonate (7.8 g, 56.25 mmol) and 4-hydroxybutylacrylate glycidylether (7.5 g, 37.5 mmol) was heated to reflux. The mixture was allowed to stir at reflux temperature for 24 hours. The mixture was cooled to room temperature and filtered to remove the undissolved potassium carbonate. The filtrate was evaporated under reduced pressure. The residual oil was diluted with ethyl acetate (250 ml) and extracted with a mixture of an aqueous solution of sodium hydroxide (1N) and distilled water (4/1). The organic layer was separated, dried over MgSO4, filtered and evaporated to provide 15.1 g of a yellow oil. The product was purified on a SVP D40 Merck Np Column using dichloromethane/n-hexane (50/50) as eluent, to afford 5.5 g of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536217B2
Source datasetuspto-grants-2013_09
ORD IDord-7d59ce6d6e374c768a9c2db1fe3fbb54
Source noteuspto-grants-2013_09