HuagongsheHuagongshe Chemistry Print Report · For research reference only
Furan → Methyl 7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Furan | HCID 8029 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | Methyl 7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylate | HCID 12271748 | — |
Reaction Steps
4.5 g (0,033 Mol) AlCl3 are added to 100 g (1 Mol) ethylacrylate and dissolved with stirring. 68 g (1 Mol) furane is then added drop-wise, during cooling to 20° to 25° C. After one hour, the exothermic reaction is terminated, followed by stirring for one hour at 25° C. and 30 g water is added. The organic phase is separated. First, the non-converted furane and ethylacrylate is distilled off under a pressure of 10 Torr. The 2-carbomethoxy-7-oxabicyclo(2.2.1)hept-5-ene boils at 60° C. and is obtained in a yield of 67.2 g (40% theoretical).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04555581 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-846525d9bd8440ef838bce0f75d15d64 |
| Source note | uspto-grants-1985_11 |