Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83950Generated: October 25, 2026

Water → alpha-Methylene-gamma-Butyrolactone N,N-Dimethyl Acrylamide

https://huagongshe.com/reaction/83950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantN,N-DimethylacrylamideHCID 17587—
ReactantSodium PersulfateHCID 62655—
Reactantalpha-Methylene butyrolactoneHCID 68352—
ReactantSodium Lauryl SulfateHCID 3423265—
Productalpha-Methylene-gamma-Butyrolactone N,N-Dimethyl AcrylamideHCID 86664977—

Reaction Conditions

Temperature73 °C

Reaction Steps

To a 100 mL round bottom flask equipped with a magnetic stir bar was added 8.844 g (0.491 mol) water and 0.121 g (4.20×10−4 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 2.053 g (2.09×10−2 mol) α-methylene-γ-butyrolactone and 2.113 g (2.13×10−2 mol) N,N-dimethyl acrylamide was added via syringe pump over 120 minutes. After 10 minutes of monomer mixture addition, an aqueous mixture consisting of 16.658 g (0.925 mol) water, 0.264 g (9.15×10−4 mol) sodium dodecyl sulfate (20% aqueous solution), 0.029 g (1.22×10−4 mol) sodium persulfate, and 0.028 g of a 20% aqueous sodium hydroxide solution was added via syringe pump over 120 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 200 kDa and a polydispersity of 3.32, relative to polystyrene standards. Differential scanning calorimetry showed a first order transition at approximately 162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846817B2
Source datasetuspto-grants-2014_09
ORD IDord-96cd259451dc4b65bb5a2afe28308cbf
Source noteuspto-grants-2014_09