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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568862Generated: October 26, 2026

Acrylamide → N-Octylacrylamide Acrylamide Vinyl Sulfonate

https://huagongshe.com/reaction/568862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylamideHCID 6579—
ReactantPotassium PersulfateHCID 24412—
Reactant2-Propenamide, N-octyl-HCID 82370—
ReactantSodium vinylsulfonateHCID 3270262—
ReactantSodium Lauryl SulfateHCID 3423265—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductN-Octylacrylamide Acrylamide Vinyl SulfonateHCID 86742029—

Reaction Steps

A one liter Morton style resin kettle, fitted with a chilled water condenser, thermometer, nitrogen sparger and mechanical stirrer was charged with 500 ml of purified water. The water was refluxed for 1 hour with a nitrogen purge and then cooled to room temperature. Acrylamide, 9.886 g (0.14 mole), 4.81 g (0.37 mole) of sodium vinyl sulfonate as a 25% solution in water, 0.33 g (0.002 mole) of N-octylacrylamide and 15 g of sodium dodecyl sulfate (SDS) were charged into the flask. The reaction solution was heated to 50° C. and 0.01 g potassium persulfate was added. After 17 hours at 50° C. and 300 rpm stirring, the viscous solution was slowly poured into 3 L of methanol and the precipitated polymer was isolated by filtration. The polymer was then masticated in a Waring blender with 2 L of methanol for 30 seconds, filtered and dried under vacuum at room temperature. The yield of the polymer was 10.9 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04730028
Source datasetuspto-grants-1988_03
ORD IDord-bd2c09e4fa2941e1be28610657c18648
Source noteuspto-grants-1988_03