HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 589225Erstellt: 26. Oktober 2026
Hydrochloric Acid → {3-(Triallylsilyl)propyl}(methoxy)dimethylsilane
https://huagongshe.com/reaction/589225
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Dimethoxydimethylsilane | HCID 66187 | — |
| Edukt | HCID 178460902 | HCID 178460902 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | {3-(Triallylsilyl)propyl}(methoxy)dimethylsilane | HCID 86726597 | 72% |
Reaktionsschritte
Under a nitrogen atmosphere, dimethoxydimethylsilane (31) (1.0 ml, 7.0 mmol) was added to a reaction container, cooled down to 0° C., diethyl ether solution of 0.72M 3-(triallylsilyl)propylmagnesium bromide (24) (19.44 mL, 14 mmol) was added dropwise. After the dropwise adding, stirring was continued at room temperature for 5 hours. To the reaction mixture, water was added to stop the reaction, then 10% hydrochloric acid was added until the salt was completely dissolved. The obtained organic layer was separated and the obtained water layer was extracted with diethyl ether. The collected organic layer was washed each with saturated sodium bicarbonate aqueous solution and saturated saline solution in this order, dried over anhydrous magnesium sulfate, then filtered, concentrated under reduced pressure, obtaining {3-(triallylsilyl)propyl}(methoxy)dimethylsilane (32) represented by the following chemical reaction equation (yield: 1.5 g, yield (%): 72%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09228107B2 |
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| Quelldatensatz | uspto-grants-2016_01 |
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| ORD ID | ord-f1016c2e3f194fe49a9a49c06728a2d7 |
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| Quellennotiz | uspto-grants-2016_01 |
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