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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 1-benzyl-5-(1,3-dithiol-2-ylidene)-3-methyl-4,6-dioxopiperidine-3-carboxylate | HCID 20204022 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Benzyl-3-(1,3-dithiol-2-ylidene)-5-methyl-2,4-dioxopiperidine | HCID 13606568 | 69.1% |
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
| 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-628112997dbd4cf6af8955a1426eba4e |
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| Source note | uspto-grants-1987_05 |
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