HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103960Generated: October 31, 2026
Carbon Disulfide → Silane, (3-isothiocyanatopropyl)trimethoxy-
https://huagongshe.com/reaction/2103960
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Aminopropyltrimethoxysilane | HCID 83756 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Silane, (3-isothiocyanatopropyl)trimethoxy- | HCID 9813262 | — |
Reaction Steps
In a reaction container mixed were 53.8 g of 3-(trimethoxysilyl)propylamine and 600 ml of dry tetrahydrofuran (THF), with cooling to 0° C. To this solution, 34.2 g of carbon disulfide was added dropwise, and the mixture was stirred at 0° C. for 5 hours in a nitrogen atmosphere. Then, a solution of 61.9 g of dicyclohexyl carbodiimide in 180 ml of dry THF and 3 g of triethylamine were added thereto, and the mixture was allowed to react at 40° C. for 5 hours. THF was removed from the reaction mixture obtained, and the residue was extracted with n-hexane. Then n-hexane was removed from the extract under reduced pressure, and the residue was distilled under reduced pressure, to obtain γ-isothiocyanatopropyltrimethoxysilane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576167B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-ff43784520554857a70815b01f56c04f |
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| Source note | uspto-grants-2009_08 |
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