HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15244Generated: October 26, 2026
1,3-Dithiolane-2-thione → 2,2'-[Thiobis(methylene)]bis-1,4,6,9-tetrathiaspiro[4.4]nonane
https://huagongshe.com/reaction/15244
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dithiolane-2-thione | HCID 13196 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | 1,1'-Thiobis(2,3-epithiopropane) | HCID 10976066 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2'-[Thiobis(methylene)]bis-1,4,6,9-tetrathiaspiro[4.4]nonane | HCID 59341515 | 4.7% |
Reaction Steps
A mixture of ethylene trithiocarbonate (5.04 g, 0.037 moles) and tetrafluoroboric acid (1.0 ml) in anhydrous dichloromethane (50.0 ml) cooled to −5° C. and stirred under nitrogen, was treated dropwise with a solution of 2,2′-[thiobis(methylene)]bis-thiirane (3.34 g, 0.019 moles) in anhydrous dichloromethane (30.0 ml). The resulting mire was allowed to warm to room temperature and quenched with 5% sodium bicarbonate solution (50.0 ml). The separation of the organic layer followed by water washing, drying and evaporation afford a wet yellow solid. Purification of which by short-path chromatography (20% ethyl acetate/hexane over silica) afforded 2,2′-[thiobis(methylene)]bis-1,4,6,9-tetrathiaspiro[4.4]nonane (4.7% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732507B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-d26563509c44439d949701404d266712 |
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| Source note | uspto-grants-2010_06 |
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