HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → Tert-butyl (1,2-diethyl-4-pyrazolidinylidene)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,2-Diethylhydrazine dihydrochloride | HCID 24372 | — |
| Reactant | Tert-butyl 4-chloro-3-(chloromethyl)-2-butenoate | HCID 18379383 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Tert-butyl (1,2-diethyl-4-pyrazolidinylidene)acetate | HCID 86584278 | 82.4% |
Reaction Steps
A suspension of tert-butyl 4-chloro-3-(chloromethyl)-2-butenoate (1.2 g, 5.3 mmol), potassium carbonate (4.0 g, 29 mmol), diethylhydrazine dihydrochloride (1.3 g, 8.0 mmol) and potassium iodide (0.86 g, 5.2 mmol) in acetonitrile was stirred at room temperature for 3 days. The mixture was filtered through celite, concentrated and purified by flash chromatography on silica gel eluting ethyl acetate:hexane (20:80, v;v) to give the tert-butyl (1,2-diethyl-4-pyrazolidinylidene)acetate (1.05 g, 82%) as an oil, MS (M+H)+=241.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06495565B2 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-e3c9e8064684428cba98fb3a9db442bf |
| Source note | uspto-grants-2002_12 |