HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589227Generated: October 26, 2026
Hydrochloric Acid → Bis{3-(triallylsilyl)propyl}(methoxy)methylsilane
https://huagongshe.com/reaction/589227
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Trimethoxymethyl silane | HCID 101924291 | — |
| Reactant | HCID 178460902 | HCID 178460902 | — |
| Solvent | Water | HCID 962 | — |
| Product | Bis{3-(triallylsilyl)propyl}(methoxy)methylsilane | HCID 131734460 | 62% |
Reaction Steps
Under a nitrogen atmosphere, trimethoxymethylsilane (18) (42 μl, 0.3 mmol) was added into a reaction container, cooled down to 0° C. and then diethyl ether solution of 0.9M 3-(triallylsilyl)propylmagnesium bromide (24) (1 mL, 0.9 mmol) was dropped. After dropping, stirring was continued at room temperature for 5 hours. To the reacted 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, then dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, obtaining bis{3-(triallylsilyl)propyl}(methoxy)methylsilane (35) represented by the following chemical reaction equation (yield: 85 mg, yield (%): 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09228107B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-7880462910c048e7bddbc15f0f4a2f52 |
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| Source note | uspto-grants-2016_01 |
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