HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657287Generated: November 2, 2026
Sodium Iodide → N-[4-diethylamino-1,1-dimethyl-2-butynyl]-4,4-diphenyl-2-cyclopentenylamine
https://huagongshe.com/reaction/1657287
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 4,4-Diphenyl-2-cyclopentenyl chloride | HCID 10753484 | — |
| Reactant | 4-Diethylamino-1,1-dimethyl-2-butynylamine | HCID 53846821 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-[4-diethylamino-1,1-dimethyl-2-butynyl]-4,4-diphenyl-2-cyclopentenylamine | HCID 19787466 | 59.3% |
Reaction Steps
A mixture of 4,4-diphenyl-2-cyclopentenyl chloride (0.60 g), 4-diethylamino-1,1-dimethyl-2-butynylamine (0.79 g) and a catalytic amount of sodium iodide in acetone (5 ml) was refluxed for 8 hours. After being cooled, the solvent was removed off under reduced pressure and the residue was purified with column chromatography on silica gel with a mixture of chloroform and methanol as an eluent to give N-[4-diethylamino-1,1-dimethyl-2-butynyl]-4,4-diphenyl-2-cyclopentenylamine (0.54 g). The free amine obtained above was dissolved in chloroform, and to the solution was added hydrogen chloride in methanol (0.18 g/ml, 1 ml). The solution was evaporated in vacuo and triturated with a mixture of ethanol and isopropyl alcohol to give its hydrochloride (0.45 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05256824 |
|---|
| Source dataset | uspto-grants-1993_10 |
|---|
| ORD ID | ord-9ba77c91ab904f1590191cd4b543f3ac |
|---|
| Source note | uspto-grants-1993_10 |
|---|