HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081223Generated: October 25, 2026
N-vinyl-2-pyrrolidone → Isooctyl Acrylate N-vinyl-2-pyrrolidone
https://huagongshe.com/reaction/1081223
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-vinyl-2-pyrrolidone | HCID 6917 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | Isooctyl acrylate | HCID 165746 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Isooctyl Acrylate N-vinyl-2-pyrrolidone | HCID 44150239 | — |
Reaction Steps
Isooctyl acrylate (54.9 Kg), N-vinyl-2-pyrrolidone (5.4 Kg), and ethyl acetate (93.6 Kg) were charged into a 75 gallon (285 liter) stainless steel reactor. The mixture was deoxygenated and heated to 55° C. After 5 minutes at 55° C., azobisisobutyronitrile (30 g) premixed in ethyl acetate (1 Kg) was charged to the reactor. Additional portions of azobisisobutyronitrile (30 g) premixed with ethyl acetate (1 Kg) were added 4 hours after the start of the reaction and again at 8 hours. The temperature was maintained at 55° C. throughout the reaction. The reaction was continued until complete. An antioxidant (61 g, IRGANOX™ 1010, Ciba-Geigy Corp.) and heptane (66.3 Kg) were added to the reactor and the contents mixed until homogeneous. The final copolymer had a measured inherent viscosity of 1.67 deciliter/g in ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05585111 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-31f64f604f5f4248a32fa774bf29c4a0 |
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| Source note | uspto-grants-1996_12 |
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