HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373724Generated: October 25, 2026
Chloro-methoxy-dimethylsilane → tert-Butylmethoxydimethylsilane
https://huagongshe.com/reaction/2373724
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloro-methoxy-dimethylsilane | HCID 74579 | — |
| Reactant | HCID 178418310 | HCID 178418310 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butylmethoxydimethylsilane | HCID 11446417 | — |
Reaction Steps
To the silane mixture comprising dimethylmethoxychlorosilane as produced by the disproportionation reaction in (a) above, was added 150 ml of toluene to dissolve the silanes in toluene, and to give a toluene solution of said silane mixture. To the toluene solution was added dropwise the THF solution of tert-butyl magnesium chloride as produced in Example 20, through a dropping funnel, at 40° C.-50° C. over 1 hour. Then, the resulting mixture was stirred at 70° C. for 4 hours. The Grignard reagent could react with dimethylmethoxychlorosilane contained in the said toluene solution, to produce tert-butyldimethylmethoxysilane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07459577B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-abad8f7dc58744d1849d429e08e49e53 |
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| Source note | uspto-grants-2008_12 |
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