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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429120Generated: November 3, 2026

Phenyltrichlorosilane → HCID 68386487, compound

https://huagongshe.com/reaction/1429120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyltrichlorosilaneHCID 7372—
Reactant1-Bromo-3,5-di-tert-butylbenzeneHCID 620136—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductHCID 68386487HCID 6838648781.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937195B2
Source datasetuspto-grants-2015_01
ORD IDord-1e359be4d1be48afabc0e3f7d60f76f9
Source noteuspto-grants-2015_01