HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991955Generated: November 2, 2026
Sodium Sulfide → 3,14-Dioxa-8,9-dithia-4,13-disilahexadecane, 4,4,13,13-tetraethoxy-
https://huagongshe.com/reaction/991955
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | (3-Chloropropyl)triethoxysilane | HCID 78771 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3,14-Dioxa-8,9-dithia-4,13-disilahexadecane, 4,4,13,13-tetraethoxy- | HCID 92506 | — |
Reaction Steps
17.8 kg of virtually anhydrous sodium sulfide are mixed with 190 l of ethanol and added to an enameled 500 l capacity reactor. This is followed by the addition through a fine nozzle of 13.85 kg of sulfur in molten form. The mixture is heated to 50° C. and 190 l of 3-chloropropyltriethoxysilane are metered in within 10 minutes. On account of the exothermic reaction the temperature of the reactor contents rises to 74° C. A further 4.45 kg of virtually anhydrous sodium sulfide are added at this temperature. Three further portions of sodium sulfide are added at 5 minute intervals (i.e. each 5 minutes), the temperature of the reactor contents rising to 82° C. After completion of the sodium sulfide addition the reaction mixture is kept for 1.5 hours at 82-83° C. and the sodium chloride that has precipitated is separated after cooling the mixture. A yellow product is obtained after evaporating the reaction mixture in vacuo and renewed fine filtration. HPLC analysis confirms the presence of a product with a mean polysulfane chain length of 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06465672B2 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-bdddaa50fe714a9893bdfe247ed5b474 |
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| Source note | uspto-grants-2002_10 |
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