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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631642Generated: November 4, 2026

Triphenylphosphine → ((2-Fluoro-5-nitrophenyl)ethynyl)trimethylsilane

https://huagongshe.com/reaction/1631642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2-Bromo-1-fluoro-4-nitrobenzeneHCID 69699—
Catalystpalladium(II) acetateHCID 167845—
SolventTriethylamineHCID 8471—
Product((2-Fluoro-5-nitrophenyl)ethynyl)trimethylsilaneHCID 12687357—

Reaction Steps

1.126 ml of ethynyl(trimethyl)silane, 55 mg of triphenylphosphine and 24 mg of palladium (2+) acetate are added to a solution of 1.169 g of 2-bromo-1-fluoro-4-nitrobenzene in 13 ml of triethylamine with stirring and under argon. After four and a half hours at a temperature of 100° C., the reaction medium is cooled and the insoluble material is filtered off through sintered glass. The filtrate is concentrated to dryness under reduced pressure. After two silica column purifications, eluent: 90/10 heptane/EtOAc then 95/5 heptane/EtOAc, 460 mg of [(2-fluoro-5-nitrophenyl)ethynyl](trimethyl)silane are obtained in the form of a yellow solid, the characteristics of which are the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791255B2
Source datasetuspto-grants-2014_07
ORD IDord-fddc04b335264f26b5c02bcd37500b85
Source noteuspto-grants-2014_07