Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83946Generated: October 26, 2026

Water → alpha-Methylene-gamma-butyrolactone n-butyl acrylate acrylic acid

https://huagongshe.com/reaction/83946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcrylic AcidHCID 6581—
ReactantButyl AcrylateHCID 8846—
ReactantSodium HydroxideHCID 14798—
ReactantSodium PersulfateHCID 62655—
Reactantalpha-Methylene butyrolactoneHCID 68352—
ReactantSodium Lauryl SulfateHCID 3423265—
Productalpha-Methylene-gamma-butyrolactone n-butyl acrylate acrylic acidHCID 86762800—

Reaction Conditions

Temperature73 °C

Reaction Steps

To a 100 mL round bottom flask equipped with a magnetic stir bar was added 8.819 g (0.490 mol) water and 0.116 g (4.02×10−4 mol) sodium dodecyl sulfate (20% aqueous solution). The mixture was heated under flowing nitrogen to 73° C., at which time a monomer mixture consisting of 2.102 g (2.14×10−2 mol) α-methylene-γ-butyrolactone, 2.102 g n-butyl acrylate (1.64×10−2 mol) and 0.220 g (3.66×10−3 mol) acrylic acid was added via syringe pump over 115 minutes. After 10 minutes of monomer mixture addition, an aqueous mixture consisting of 16.711 g (0.928 mol) water, 0.267 g (9.26×10−4 mol) sodium dodecyl sulfate (20% aqueous solution), 0.026 g (1.09×10−4 mol) sodium persulfate, and 0.033 g of a 20% aqueous sodium hydroxide solution was added via syringe pump over 115 minutes. After both the monomer and aqueous mixtures were added completely, the emulsion was allowed to stir for an additional 60 minutes, after which the reaction was cooled to room temperature and dried under vacuum under vacuum at 90° C. overnight. Size exclusion chromatography yielded a monomodal peak with a weight average molecular weight of 296 kDa and a polydispersity of 2.84, relative to polystyrene standards. Differential scanning calorimetry showed a single first order transition at approximately 21° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846817B2
Source datasetuspto-grants-2014_09
ORD IDord-cdc9bdf1d81248c0ac5eda949b703853
Source noteuspto-grants-2014_09