HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368963Generated: October 26, 2026
N-vinyl-2-pyrrolidone → Isooctyl acrylate 2-Hydroxyethyl acrylate N-vinyl-2-pyrrolidone
https://huagongshe.com/reaction/368963
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-vinyl-2-pyrrolidone | HCID 6917 | — |
| Reactant | 2-Hydroxyethyl acrylate | HCID 13165 | — |
| Reactant | 2,2'-Azobis(2-methylbutyronitrile) | HCID 93079 | — |
| Reactant | Isooctyl acrylate | HCID 165746 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Isooctyl acrylate 2-Hydroxyethyl acrylate N-vinyl-2-pyrrolidone | HCID 86755949 | — |
Reaction Steps
A flask equipped with an agitator, condenser, nitrogen inlet tube and an addition funnel was charged with isooctyl acrylate (155.75 g), N-vinyl-2-pyrrolidone (15.75 g) and hydroxyethyl acrylate (3.50 g) premixed in a mixture of ethyl acetate (249.38 g) and methanol (13.13 g). 2,2'-Azobis-(2-methyl-butyronitrile) (0.26 g, Wako™ V-59) was added to initiate reaction. The mixture was purged with nitrogen to remove oxygen. The mixture was agitated and heated to 57° C. and the reaction was run for about 24 hours at this temperature. After termination of the reaction additional ethyl acetate (178.13 g) and methanol (9.38 g) were added. The inherent viscosity was 1.27 dl/g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06136807 |
|---|
| Source dataset | uspto-grants-2000_10 |
|---|
| ORD ID | ord-be63899eadfc4337af3324fb6d4c1de3 |
|---|
| Source note | uspto-grants-2000_10 |
|---|