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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantSodium hydrideHCID 24758—
Reactantcis-1,2-DichloroethyleneHCID 643833—
Reactant1-Benzylpiperidine-2,4-dioneHCID 22495541—
SolventDimethyl SulfoxideHCID 679—
Product1-Benzyl-3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04663319
Source datasetuspto-grants-1987_05
ORD IDord-cb7aef7f2e6e4f0a93b9032debeec418
Source noteuspto-grants-1987_05