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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165754Generated: October 25, 2026

Chlorotrimethylsilane → ((3-Bromophenyl)ethynyl)trimethylsilane

https://huagongshe.com/reaction/1165754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Bromo-3-ethynylbenzeneHCID 11480818—
ReactantHCID 86605439HCID 86605439—
SolventTetrahydrofuranHCID 8028—
Product((3-Bromophenyl)ethynyl)trimethylsilaneHCID 3683324—

Reaction Conditions

Temperature25 °C

Reaction Steps

Under an inert atmosphere, 9.5 g of the compound of Step A were introduced into 100 g of tetrahydrofuran, and at 25° C.±3° C., over 15 minutes, 69 ml of a 0.8M solution of magnesium ethyl bromide were added, with stirring for 15 minutes at 25° C. Then, over 2 minutes and without cooling, 8 ml of trimethylsilyl chloride were added with stirring for 30 minutes at 25° C. The reaction mixture was poured into a 2M aqueous solution of NH4Cl and was extracted with ether, dried, filtered, and the filtrate was concentrated to dryness by distilling under reduced pressure then rectified to obtain 12.1 g of 3-(trimethylsilylethynyl)bromobenzene with a boiling point at 0.05 mm/Hg=78° to 84° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04912097
Source datasetuspto-grants-1990_03
ORD IDord-b45ad6403f1a42f39b80f269ce0cdad9
Source noteuspto-grants-1990_03