HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylic Acid → Octyl acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | 2-Ethylhexanoic Acid | HCID 8697 | — |
| Reactant | 2-Hydroxyethyl acrylate | HCID 13165 | — |
| Reactant | 2-Octynoic acid | HCID 21872 | — |
| Reactant | 2,2-Dimethoxy-2-phenylacetophenone | HCID 90571 | — |
| Product | Octyl acrylate | HCID 17258 | — |
Reaction Steps
The acrylic monomers generated in Examples 1 and 10-12, 2-OA, 2-EHA, and LA were each prepared into adhesive films using the following procedure. The alkyl acrylate (28.5 g), 0.02 g of IRGACURE 651 (Ciba), 0.3 g of acrylic acid (AA, Alfa Aesar), and 1.2 g of hydroxyethyl acrylate (HEA, Aldrich) were mixed using a magnetic stir bar in a clear glass vial. The glass vial was then purged with nitrogen for 5 minutes to remove dissolved oxygen, and then treated with UV light (365 nm, approximately 5 mW/cm2) until a coatable viscosity was achieved. The target for this step was an approximate viscosity of 3000 cP at room temperature and acrylic conversion of approximately 10%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09102774B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-9403597690d84694b750eb9d6eb78775 |
| Source note | uspto-grants-2015_08 |