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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 873692Erstellt: 25. Oktober 2026

1-Bromo-4-iodobenzene → HCID 12169538, Verbindung

https://huagongshe.com/reaction/873692

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-4-iodobenzeneHCID 11522—
Edukt1,1'-BinaphthylHCID 11789—
Edukt4-BenzylpiperidineHCID 31738—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 12169538HCID 12169538—

Reaktionsschritte

A mixture of 1-bromo-4-iodo benzene (0.500 g), 4-benzylpiperidine (0.25 mL), sodium-tert-butylate (0.238 g), tris(dibenzylideneacetone)dipalladium (0.016 g) and 2,2′-bis/diphenylphosphino)-1,1′-binaphtyl racemate (0.018 g) is dissolved in tetrahydrofuran and stirred at room temperature overnight. The reaction mixture is concentrated and the resulting residue is loaded on Celite and purified by silica gel chromatography (4:1 hexanes/ethyl acetate) to give 4-benzyl-1-(4-bromo-phenyl)-piperidine as a light yellow syrup. MS (m/z): 331 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08975439B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-5faeecc2351246c99104ab2c5f4c10c6
Quellennotizuspto-grants-2015_03