HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 1-(1,3-Dithiol-2-ylidene)-2-carbamoylpyrrolidinium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | L-Prolinamide | HCID 111306 | — |
| Reactant | (2H-1,3-Dithiol-2-ylidene)(methyl)sulfanium iodide | HCID 19751531 | — |
| Solvent | Acetone diethylether | HCID 21584533 | — |
| Product | 1-(1,3-Dithiol-2-ylidene)-2-carbamoylpyrrolidinium iodide | HCID 13729824 | 53% |
Reaction Steps
To 30 ml of tetrahydrofuran, 1.6 g of proline amide was dissolved, and 2.0 g of 2-methylthio-1,3-dithiolium iodide was gradually added under stirring at room temperature. The mixture was stirred at room temperature for 1 hour, and the precipitated crystals were collected by filtration and recrystallized from acetone-ethyl ether, whereby 1.3 g (yield: 53%) of 1-(1,3-dithiol-2-ylidene)-2-carbamoylpyrrolidinium iodide (Compound No. 44) was obtained as crystals having a melting point of from 250° to 251° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04737494 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-3069e48ee76644c89f678b1f04d6eaa5 |
| Source note | uspto-grants-1988_04 |