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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 724633Erstellt: 24. Oktober 2026

1,1'-Biphenyl, 4-(bromomethyl)- → 1-(2-Biphenyl-4-yl-1-phenyl-ethyl)-1H-benzotriazole

https://huagongshe.com/de/reaction/724633

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-Biphenyl, 4-(bromomethyl)-HCID 257716—
Edukt1-Benzyl-1H-benzotriazoleHCID 521212—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(2-Biphenyl-4-yl-1-phenyl-ethyl)-1H-benzotriazoleHCID 2187951383%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A solution of 1-benzyl-1H-1,2,3-benzotriazole (750 mg, 3.6 mmol) in tetrahydrofuran (36 mL) was cooled to −78° C. and treated with n-butyllithium (2.8 mL, 1.6 M in hexanes) dropwise. The reaction mixture was stirred at −78° C. for 10 min and 4-bromomethyl-biphenyl (1.0 g, 4.1 mmol) in tetrahydrofuran (4 mL) was added dropwise. The reaction mixture was stirred at −78° C. for 1 h, quenched with sat. ammonium chloride (100 mL), and extracted with ethyl acetate (150 mL). The organic layer was separated and washed with brine (50 mL), dried with sodium sulfate, filtered, and concentrated to a white solid. This material was triturated with diethyl ether (2×50 mL) to yield the desired product (1.12 g, 83%). LCMS found for C26H22N3 (M+H)+: m/z=376.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07141596B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-1d742bfcfbad42edb21b57e3f9c1a024
Quellennotizuspto-grants-2006_11