HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977967Generated: October 30, 2026
Water → 1-Benzyl-5-(1,3-dithiol-2-ylidene)-4,6-dioxopiperidine-2,3-dicarboxylic acid diethyl ester
https://huagongshe.com/reaction/977967
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Diethyl Maleate | HCID 5271566 | — |
| Reactant | ethyl 2-(1,3-dithiol-2-ylidene)-2-(N-benzylcarbamoyl)acetate | HCID 20204019 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Benzyl-5-(1,3-dithiol-2-ylidene)-4,6-dioxopiperidine-2,3-dicarboxylic acid diethyl ester | HCID 13934865 | — |
Reaction Steps
A mixture of ethyl 2-(1,3-dithiol-2-ylidene)-2-(N-benzylcarbamoyl)acetate (1.0 g) and dimethylformamide (25 ml) is added dropwise to a suspension of sodium hydride (63% dispersion in oil, 144 mg) in dimethylformamide (10 ml). Said addition is carried out under ice-cooling. The mixture is stirred at the same temperature for 30 minutes. A solution of diethyl maleate (0.6 ml) in dimethylformamide (10 ml) is added dropwise thereto. The mixture is stirred at room temperature overnight. The mixture is poured into water, and extracted with ethyl acetate. The extract is washed with a saturated sodium chloride solution, dried and then distilled to remove the solvent. The mixture is purified by silica gel column chromatography (solvent, n-hexane:ethyl acetate=1:2) to give 1-benzyl-5-(1,3-dithiol-2-ylidene)-4,6-dioxopiperidine-2,3-dicarboxylic acid diethyl ester (196 mg) as yellow oil.
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-35f0fa3623704988a3d6f07dca1323b3 |
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| Source note | uspto-grants-1987_05 |
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