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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411817Generated: October 27, 2026

Chlorotrimethylsilane → (5-Bromo-1,3-phenylene)bis(trimethylsilane)

https://huagongshe.com/reaction/411817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant1,3,5-TribromobenzeneHCID 12279—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product(5-Bromo-1,3-phenylene)bis(trimethylsilane)HCID 12884904141.4%

Reaction Conditions

Temperature-70 °C

Reaction Steps

1,3,5-Tribromobenzene (125 g, 0.4 mol), was dissolved in anhydrous diethylether (1 L), and cooled to −70° C. n-Butyllithium (250 mL, 1.6 M in hexanes, 0.4 mol) was added dropwise over a one-hour period keeping the temperature near −70° C. The solution was stirred for an additional 20 minutes at −70° C. and then warmed to −10° C. over a two-hour period. The solution was then recooled to −70° C. and trimethylchlorosilane (45 g, 0.4 mol) was added over a one hour period. The solution was allowed to stir and warm to room temperature overnight. The solution was cooled to −70° C. and an additional 0.4 mol n-butyl lithium was added over a one-hour period. The resulting slurry was stirred for one hour at −70° C., warmed to −10° C. over a two-hour period and then recooled to −70° C. An additional 0.4 mol of trimethylchlorosilane was added and the slurry was allowed to warm to room temperature overnight. The mixture was quenched with water and the layers were separated. The organic layer was washed twice with sodium bicarbonate solution and with salt brine then dried over magnesium sulfate. The solvents were evaporated under vacuum and the product distilled twice under vacuum to yield 85.2 g (70%) of a colorless liquid. b.p. 100-105° C. @ 0.5 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559262B1
Source datasetuspto-grants-2003_05
ORD IDord-9da823d4b62b45bdb197c72e0744401e
Source noteuspto-grants-2003_05