HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977946Generated: October 30, 2026
Methyl iodide → 1-Methyl-3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidine
https://huagongshe.com/reaction/977946
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(1,3-Dithiol-2-ylidene)-2,4-dioxopiperidine | HCID 13606562 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Methyl-3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidine | HCID 13606563 | 59.5% |
Reaction Steps
Sodium hydride (60% dispersion in oil) (226 mg) is suspended in N,N-dimethylformamide (10 ml), and to the suspension is added dropwise a solution of 3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidine (1.0 g) (which is prepared in Example 13) in N,N-dimethylformamide (100 ml) while cooling at 0° to 5° C. The mixture is stirred for 10 minutes at the same temperature, and to the mixture is added dropwise methyl iodide (861 mg), and the mixture is stirred at 0° to 2° C. for 1.5 hour. After distilling off the solvent under reduced pressure, the residue is purified by silica gel column chromatography (solvent, n-hexane:ethyl acetate=1:1), and recrystallized from ethyl acetate-isopropyl ether to give 1-methyl-3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidine (634 mg, 59.5%) as pale yellow needles. m.p. 148.5°-153° 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-5d3bcf8875ab4c29afdd69d1423c9708 |
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| Source note | uspto-grants-1987_05 |
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