HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(4-hexadecylamino-2-thiophenecarbonyl)pyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 4-[N-(carbobenzyloxy)-N-hexadecylamino]-2-thiophenecarbonyl chloride | HCID 20503621 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-(4-hexadecylamino-2-thiophenecarbonyl)pyrrolidine | HCID 20503634 | — |
Reaction Steps
A warm solution of 1.0 g. of 4-[N-(carbobenzyloxy)-N-hexadecylamino]-2-thiophenecarbonyl chloride and 1.3 g. of triethylamine in 100 ml. of ether is added to 1.2 g. of pyrrolidine. A precipitate forms; the mixture is stirred under reflux for 1 hour, filtered, and extracted with hot ether. The extract is evaporated and a solution of the resulting residue in 100 ml. of tetrahydrofuran is shaken under 50 psi of hydrogen in the presence of 0.6 g. of 10% palladium on carbon. The mixture is filtered and the filtrate evaporated. The residue is crystallized from acetic acid to yield the product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04382143 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-182954555e6c418c85361989a6b34cc9 |
| Source note | uspto-grants-1983_05 |