HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977950Generated: October 27, 2026
Carbon Disulfide → 1-Benzyl-3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidine
https://huagongshe.com/reaction/977950
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | cis-1,2-Dichloroethylene | HCID 643833 | — |
| Reactant | 1-Benzylpiperidine-2,4-dione | HCID 22495541 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-Benzyl-3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidine | HCID 13606559 | — |
Reaction Steps
Sodium hydride (60% despersion in oil) (432 mg) is suspended in dimethylsulfoxide (10 ml), and to the suspension is added dropwise a solution of 1-benzyl-2,4-dioxopiperidine (1.0 g) and carbon disulfide (0.33 ml) in dimethylsulfoxide (20 ml). The mixture is stirred for 2 hours, and thereto is added dropwise a solution of cis-1,2-dichloroethylene (0.42 ml) in dimethylsulfoxide (5 ml). The mixture is stirred at room temperature for 1.5 hour and further at 50° C. for 1 hour. The reaction mixture is poured onto water and extracted with benzene. The extract is washed with water, dried and then distilled to remove the solvent. The residue is recrystallized from isopropyl alcohol to give 1-benzyl-3-(1,3-dithiol-2-ylidene)-2,4- dioxopiperidine (486 mg) as pale yellow needles. m.p. 122°-124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04663319 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-cb7aef7f2e6e4f0a93b9032debeec418 |
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| Source note | uspto-grants-1987_05 |
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