HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → Oxolan-2-yl 1-ethenyl-2-oxopyrrolidine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Furan, 2-chlorotetrahydro- | HCID 178730 | — |
| Reactant | HCID 15389820 | HCID 15389820 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Oxolan-2-yl 1-ethenyl-2-oxopyrrolidine-3-carboxylate | HCID 54014762 | — |
Reaction Steps
8.9 g or 3-(t-butoxycarbonyl)-1-vinyl-2-pyrrolidinone (BCVP) was dissolved in 50 ml of tetrahydrofuran free of moisture. To this solution 1.0 g of sodium hydride and 4.4 g of 2-chlorotetrahydrofuran were added and allowed to react at room temperature for 1 hour. This solution was diluted with diethylether and washed many times with pure water. The organic solvent of the organic phase was evaporated and the residue was subjected to silica gel column chromatography, to obtain 9.3 g of pure 3-(tetrahydrofuranyloxycarbonyl)-1-vinyl-2-pyrrolidinone (hereinafter referred to as “TFVP”). Its chemical structure was determined by IR spectra and NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06262222B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-6fdd0a8cf79049a5b451472014cfbef5 |
| Source note | uspto-grants-2001_07 |