HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429120Generated: November 3, 2026
Phenyltrichlorosilane → HCID 68386487, compound
https://huagongshe.com/reaction/1429120
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyltrichlorosilane | HCID 7372 | — |
| Reactant | 1-Bromo-3,5-di-tert-butylbenzene | HCID 620136 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 68386487 | HCID 68386487 | 81.8% |
Reaction Steps
Under a nitrogen atmosphere, to a diethyl ether solution (106 mL) of 1-bromo-3,5-di-tert-butylbenzene (10.60 g, 39.37 mmol), a 1.65 M hexane solution of n-butyllithium (23.86 mL, 39.37 mmol) was added dropwise at −78° C. After the mixture was gradually warmed to room temperature, stirring was performed at room temperature for 3 hours. The resultant mixture was added dropwise to a diethyl ether solution (106 mL) of trichlorophenylsilane (24.99 g, 118.12 mmol) at −78° C. After the mixture was gradually warmed to room temperature, stirring was performed at room temperature. After completion of the reaction, the solvent was removed under reduced pressure. Thereafter, hexane wad added to the residue, and insoluble materials were removed by filtration. The solvent was removed from the filtrate under reduced pressure. Trichlorophenylsilane was removed by heating to 100° C. under reduced pressure to obtain dichloro(3,5-di-tert-butylphenyl)(phenyl)silane (11.77 g, yield 81.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937195B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-1e359be4d1be48afabc0e3f7d60f76f9 |
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| Source note | uspto-grants-2015_01 |
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