HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 1-Benzyl-3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (2H-1,3-Dithiol-2-ylidene)(methyl)sulfanium iodide | HCID 19751531 | — |
| Reactant | 1-Benzylpiperidine-2,4-dione | HCID 22495541 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Benzyl-3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidine | HCID 13606559 | 87.8% |
Reaction Steps
Sodium hydride (60% dispersion in oil) (80 mg) is suspended in tetrahydrofuran (10 ml), and thereto are added 1-benzyl-2,4-dioxopiperidine (200 mg) and 2-methylthio-1,3-dithiolium iodide (273 mg). The mixture is stirred at room temperature for 30 minutes. The reaction mixture is poured onto water and extracted with chloroform. The extract is washed with a saturated sodium chloride solution, dried and then distilled to remove the solvent. The residue is purified by silica gel column chromatography (solvent; ethyl acetate:n-hexane=1:1) and recrystallized from isopropyl alcohol to give 1-benzyl-3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidine (262 mg, 87.8%) as pale yellow needles, m.p. 122°-124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04663319 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-5df2db783bb24444a96293ab58b974af |
| Source note | uspto-grants-1987_05 |