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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 244382Erstellt: 24. Oktober 2026

Diisopropylamine → 1-(4-Trimethylsilanylethynylphenyl)propan-1-one

https://huagongshe.com/de/reaction/244382

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
EduktTrimethylsilylacetyleneHCID 66111—
Eduktp-BromopropiophenoneHCID 66312—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(4-Trimethylsilanylethynylphenyl)propan-1-oneHCID 67363127—

Reaktionsschritte

A mixture of 1.74 g 4′-bromopropiophenone, 2.0 g ethynyltrimethylsilane, 260 mg bis(triphenylphosphine)palladium(II) dichloride, 260 mg copper(I) iodide and 15 ml diisopropylamine in 40 ml tetrahydrofuran is heated at reflux for 1 h. After cooling the reaction mixture is diluted with water and extracted with ethyl acetate. The combined organic layer is washed with brine, dried over sodium sulfate and evaporated under reduced pressure. The residue is purified by chromatography on silica gel, using a mixture of heptane/ethyl acetate 9:1 as eluent to obtain 1-(4-trimethylsilanylethynylphenyl)propan-1-one, m.p. 36-37° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658644B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-3b2f550dab3f4c0b9c363fa1b256f8ef
Quellennotizuspto-grants-2014_02