HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Hydroxyethyl acrylate → 2-(Acryloyloxy)ethyl 5-carboxy-7-oxabicyclo [2.2.1]hept-2-ene-6-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Hydroxyethyl acrylate | HCID 13165 | — |
| Reactant | 3a,4,7,7a-Tetrahydro-4,7-epoxyisobenzofuran-1,3-dione | HCID 98484 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(Acryloyloxy)ethyl 5-carboxy-7-oxabicyclo [2.2.1]hept-2-ene-6-carboxylate | HCID 20464892 | — |
Reaction Steps
Maleic anhydride (50 g) and furan (150 ml) were heated under reflux for 1 hour, and then the excess of furan was distilled off. The residue was recrystallised from chloroform, yielding 72 g of 7-oxabicyclo [2.2.1]hept-2-ene-5,6-dicarboxylic acid anhydride (m.pt. 110° C., decomp.). This anhydride (40 g) and 30.75 g of 2-hydroxyethyl acrylate were heated in 250 ml of toluene at 100° C. for 3 hours, and then the toluene was distilled off under reduced pressure, leaving the desired compound as a viscous liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04440850 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-9080267a457240da87884a2010723a7e |
| Source note | uspto-grants-1984_04 |