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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842474Generated: October 25, 2026

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

https://huagongshe.com/reaction/842474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant3,5-Dibromo-1-trimethylsilylbenzeneHCID 626244—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product(5-Bromo-1,3-phenylene)bis(trimethylsilane)HCID 1288490494%

Reaction Conditions

Temperature-68 °C

Reaction Steps

17.18 g of 3,5-Dibromo-trimethylsilyl-benzene, 55.8 mmol, was dissolved in 380 ml Et2O. The solution was chilled to −68° C., and 22.3 mL of n-BuLi (2.5 M in hexanes), 55.8 mmol, were added within 18 minutes. The solution changed its color from clear to yellow, and was stirred for 45 minutes at −68° C. 7.5 mL TMSCl, 59 mmol, were added within six minutes. The temperature of solution rose within one hour to −33° C., and after another 30 minutes to −18° C. The solution was stirred overnight at room temperature. 60 mL of 2M HCl were added to the white suspension. Stirring for 30 minutes resulted in two clear phases. Et2O-phase was dried with MgSO4, filtered, and solvent evaporated. Raw product was distilled at a temperature of 70-76° C. and 0.1-0.2 mbar. All pure fractions were combined and gave 15.8 g of product (52.4 mmol, 94%). 1H-NMR (CHCl3=7.24 ppm): δ 7.56 (s, 2H), 7.50 (t, 1H), 0.25 (s, 6×3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376411B1
Source datasetuspto-grants-2002_04
ORD IDord-b6d6adb7758148b7b4f4276a68aeef52
Source noteuspto-grants-2002_04