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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44127Generated: October 26, 2026

Iodine → Dithienyldimethoxysilane

https://huagongshe.com/reaction/44127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTetramethoxysilaneHCID 12682—
Reactant2-BromothiopheneHCID 13851—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductDithienyldimethoxysilaneHCID 89573734—

Reaction Steps

With protection of nitrogen gas, 3.50 g magnesium powder, 1.30 g bromothiophene and 20 ml tetrahydrofuran were added to a 250 ml three-necked flask equipped with a stirrer, a reflux condenser tube and a thermometer. After the mixed system was refluxed for 0.5 hour, 0.26 g iodine was added until the reaction got severe. After the reaction was stable, a mixed solution of 20.74 g bromothiophene, 60 ml tetrahydrofuran and 9.99 g tetramethoxysilane was added dropwise from an upper part of tube within about 2 hours. After being heated with stirring and refluxing for 5 hours, the mixed system was slowly cooled to room temperature, filtered by a filter tube with protection of nitrogen gas, and the solid substance was washed with tetrahydrofuran several times. The resulting filtrate was subjected to distillation at normal pressure and solvent recovery, and then subjected to distillation at reduced pressure. The product at 130° C. to 131° C. and 25 mmHg column pressure were collected. Te infrared spectrum and 13C nuclear magnetic resonance spectrum of the synthesized compound are substantially identical with that in FIG. 1 and FIG. 2. The infrared spectrum preliminarily approves the occurrence of the synthetic reaction, and the 13C nuclear magnetic resonance spectrum effectively demonstrates the formation of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541332B2
Source datasetuspto-grants-2013_09
ORD IDord-3b52f5fac0984de3bbfa608528c21433
Source noteuspto-grants-2013_09