HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568862Generated: October 26, 2026
Acrylamide → N-Octylacrylamide Acrylamide Vinyl Sulfonate
https://huagongshe.com/reaction/568862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrylamide | HCID 6579 | — |
| Reactant | Potassium Persulfate | HCID 24412 | — |
| Reactant | 2-Propenamide, N-octyl- | HCID 82370 | — |
| Reactant | Sodium vinylsulfonate | HCID 3270262 | — |
| Reactant | Sodium Lauryl Sulfate | HCID 3423265 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Octylacrylamide Acrylamide Vinyl Sulfonate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04730028 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-bd2c09e4fa2941e1be28610657c18648 |
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| Source note | uspto-grants-1988_03 |
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