HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926408Generated: October 31, 2026
Dimethylcarbamoyl Chloride → HCID 20227442, compound
https://huagongshe.com/reaction/926408
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Aminopropyltrimethoxysilane | HCID 83756 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 20227442 | HCID 20227442 | 82.5% |
Reaction Steps
5.0 g (46.5 mmol) N,N-dimethylcarbamoyl chloride (Sigma-Aldrich, Switzerland) and 40 mL dried dioxane (Sigma-Aldrich, Switzerland) were added to a 250-mL round-bottom two-neck flask equipped with a reflux cooler. 4.71 g (46.5 mmol) triethylamine (Sigma-Aldrich, Switzerland) and 8.34 g (46.5 mmol) 3-aminopropyltrimethoxysilane (Silquest A-1110, Momentive Performance Materials Inc., USA) were added dropwise under nitrogen, with stirring. After the exothermic reaction subsided, the resulting whitish suspension was stirred at 90° C. for 3 hours. A gradual color change to orange was observed. After cooling to 50° C., the solid was separated by double filtration, and the solvent was removed at 60° C. for 1 hour on a rotary evaporator. 9.6 g of the desired silane was obtained as a brown liquid. The silane was designated as DMA1100 and used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284447B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-c2c7882687f04198b3b48bf9724258ff |
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| Source note | uspto-grants-2016_03 |
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