Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724633Generated: October 25, 2026

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

https://huagongshe.com/reaction/724633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-Biphenyl, 4-(bromomethyl)-HCID 257716—
Reactant1-Benzyl-1H-benzotriazoleHCID 521212—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Biphenyl-4-yl-1-phenyl-ethyl)-1H-benzotriazoleHCID 2187951383%

Reaction Conditions

Temperature-78 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141596B2
Source datasetuspto-grants-2006_11
ORD IDord-1d742bfcfbad42edb21b57e3f9c1a024
Source noteuspto-grants-2006_11