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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1008866Erstellt: 26. Oktober 2026

Triethylamine → 1-(3-Biphenyl-3-yl-1,1-dimethylprop-2-yn-1-yl)-4-(2,2-dimethylpropanoyl)piperazine

https://huagongshe.com/reaction/1008866

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3-BromobiphenylHCID 16449—
Edukt1-(2,2-Dimethylpropanoyl)-4-(1,1-dimethylprop-2-yn-1-yl)piperazineHCID 86610208—
KatalysatorTriphenylphosphineHCID 11776—
KatalysatorBis(triphenylphosphine)palladiumHCID 10122028—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(3-Biphenyl-3-yl-1,1-dimethylprop-2-yn-1-yl)-4-(2,2-dimethylpropanoyl)piperazineHCID 6730575961,7%

Reaktionsschritte

1.05 g (4.5 mmol) of 3-bromobiphenyl and 0.9 g (3.6 mmol) of 1-(2,2-dimethylpropanoyl)-4-(1,1-dimethylprop-2-yn-1-yl)piperazine, prepared in step 5.1., 0.75 ml (5.38 mmol) of triethylamine and 0.028 g (0.11 mmol) of triphenylphosphine are dissolved in 8 ml of tetrahydrofuran. Under an argon atmosphere, 0.126 g (0.18 mmol) of the dichloride complex of bis(triphenylphosphine) palladium is added. The mixture is stirred for 15 minutes and then 0.014 g (0.07 mmol) of cuprous iodide is added. The mixture is stirred at ambient temperature for 4 hours and then at 60° C. overnight. After cooling to temperature it is diluted with 25 ml of ethyl acetate and filtered on paper. The solid is rinsed with 4 times 10 ml of ethyl acetate. 4 g of silica are added to the filtrate, which is evaporated to dryness. The residue is purified by chromatography on silica gel, eluting with a 90/10 then 80/20 and 70/30 mixture of cyclohexane and ethyl acetate, to give 0.90 g (2.22 mmol) of product in the form of a orange-colored oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07973042B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-72c1a8ef385746afa76eeaa09f3a3efc
Quellennotizuspto-grants-2011_07