HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589224Generated: October 31, 2026
HCID 86726596, compound → HCID 86726593, compound
https://huagongshe.com/reaction/589224
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86726596 | HCID 86726596 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | HCID 86726593 | HCID 86726593 | 85% |
Reaction Steps
Under a nitrogen atmosphere, bis{3-(triallylsilyl)propyl}dimethoxysilane (29′) (1.0 g, 2.097 mmol) was cooled down to −78° C., then n-pentane solution of 1.61M t-butyllithium 1.954 mL (3.145 mmol) was added dropwise, then stirred at −78° C. for 17 hours. The reacted mixture was cooled down to 0° C., quenched with water, saturated ammonium chloride aqueous solution was added. The obtained organic layer was separated. The obtained water layer was extracted with diethyl ether and the collected organic layer was each washed with saturated sodium bicarbonate aqueous solution and saturated saline solution in this order, dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, obtaining a crude product. The crude product was purified through short silica gel column chromatography (eluent: hexane/ethyl acetate=20/1), obtaining bis({3-(triallylsilyl)propyl}(tert-butyl)methoxysilane (30) (yield: 0.902 g, yield (%): 85%).
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-e728f2e4e6b54abdaef300b6321eda05 |
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| Source note | uspto-grants-2016_01 |
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