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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977957Generated: October 30, 2026

Hydrochloric Acid → 1-Benzyl-3-(1,3-dithiol-2-ylidene)-5-methyl-2,4-dioxopiperidine

https://huagongshe.com/reaction/977957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 1-benzyl-5-(1,3-dithiol-2-ylidene)-3-methyl-4,6-dioxopiperidine-3-carboxylateHCID 20204022—
SolventEthanolHCID 702—
Product1-Benzyl-3-(1,3-dithiol-2-ylidene)-5-methyl-2,4-dioxopiperidineHCID 1360656869.1%

Reaction Steps

Ethyl 1-benzyl-5-(1,3-dithiol-2-ylidene)-3-methyl-4,6-dioxopiperidine-3-carboxylate (245 mg) is dissolved in ethanol (5 ml), and thereto is added a 10% sodium hydroxide solution (2.5 ml). The mixture is stirred at room temperature overnight. The mixture is acidified with 10% HCl, and poured into water. The aqueous solution is extracted with ethyl acetate. The extract is washed with a saturated sodium chloride solution, dried and then distilled to remove the solvent. The residue is dissolved in ethanol (20 ml) and the solution is refluxed for one hour. The mixture is distilled to remove the solvent. The residue is purified by silica gel column chromatography (solvent, ethyl acetate:n-hexane=1:1), and is recrystallized from a mixture of ethyl acetate and n-hexane to give 1-benzyl-3-(1,3-dithiol-2-ylidene)-5-methyl-2,4-dioxopiperidine (138 mg, 69.1%) as pale yellow needles, m.p. 168°-170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04663319
Source datasetuspto-grants-1987_05
ORD IDord-628112997dbd4cf6af8955a1426eba4e
Source noteuspto-grants-1987_05