HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451131Generated: October 26, 2026
N-vinyl-2-pyrrolidone → DMAPMA n-Octadecyl Methacrylate
https://huagongshe.com/reaction/1451131
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-vinyl-2-pyrrolidone | HCID 6917 | — |
| Reactant | Stearyl methacrylate | HCID 122600 | — |
| Reactant | Vinyl caprolactam | HCID 17881685 | — |
| Reactant | Dimethylaminopropylmethacrylamide | HCID 20976834 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | DMAPMA n-Octadecyl Methacrylate | HCID 131719863 | — |
Reaction Steps
Vinyl pyrrolidone (55.6 g), vinyl caprolactam (577.5 g), dimethylaminopropyl methacrylamide (DMAPMA) (42.6 g), n-octadecyl methacrylate (33.9 g) and ethanol (867.2 g) were charged into a 2-liter water-jacketed resin flask. The reaction flask was equipped with a condenser, a thermometer, a septum (for catalyst addition), an anchor-type metal stirrer, and a nitrogen sparge tube. Nitrogen was bubbled through the solution while the resin flask was heated to 68° C. using hot water circulating through the jacketed flask. After an additional half-hour of degassing at reflexing, a first shot of Lupersol 11 (0.25 ml) was injected into the flask. Subsequently, Lupersol 11 additions were made at 10, 40, 70, 100, 140, 180 and 240 minutes after the first addition. The reaction temperature was then brought up to 75° C. and held for an additional 5 hours, then cooled to room temperature and discharged.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05603919 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-c8ae15962ee54485b7920f023876a9d9 |
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| Source note | uspto-grants-1997_02 |
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