HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → Ethyl 2-furanacrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Diethyl Sulfate | HCID 6163 | — |
| Reactant | Tripropylamine | HCID 7616 | — |
| Reactant | 2-(Furan-2-yl)prop-2-enoic acid | HCID 316259 | — |
| Product | Ethyl 2-furanacrylate | HCID 95368 | — |
Reaction Steps
A mixture of diethylsulphate (57.41 g) and tri-n-propylamine was added dropwise with stirring to a solution of furanylacrylic acid (34.53 g) in acetone (150 ml). When the addition was complete the mixture was refluxed for six hours. The acetone was evaporated at reduced pressure. The resultant oily residue was dissolved in ethyl acetate, washed with aqueous sodium bicarbonate solution dried (MgSO4) and the solvent evaporated to yield ethyl 3-(2-furanyl)acrylate (46.7 g) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04388317 |
| Source dataset | uspto-grants-1983_06 |
| ORD ID | ord-ce3accae08514795b5bf6082e31dad32 |
| Source note | uspto-grants-1983_06 |