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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875246Generated: October 29, 2026

1-Bromopentane → 4-Bromo-4'-(pentyloxy)-1,1'-biphenyl

https://huagongshe.com/reaction/875246

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopentaneHCID 8057—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-4'-hydroxybiphenylHCID 95093—
SolventAcetoneHCID 180—
Product4-Bromo-4'-(pentyloxy)-1,1'-biphenylHCID 280138853%

Reaction Steps

Under an argon atmosphere, 4-bromo-4′-hydroxybiphenyl (3.0 g, 12 mmol), 1-bromopentane (3.6 g, 24 mmol), and potassium carbonate (1.66 g, 12 mmol) were dissolved in acetone (60 mL) and stirred under a reflux condition for 24 hours. After they reacted with each other, liquid separation and extraction were performed with water and chloroform. After an organic layer was dried with anhydrous sodium sulfate and filtered, the solvent was distilled off under a reduced pressure. After the obtained reaction mixture was separated and purified with a silica gel column chromatography using chloroform as a moving bed, the mixture was purified by a recrystallization method using chloroform and hexane. Thereby, a white solid of 4-Bromo-4′-pentyloxybiphenyl (A1) was obtained (1.99 g, yield: 53%). The obtained product (A1) was identified by using a 1H-NMR method. 1H-NMR (CDCl3, 400 MHz) δ=7.53-7.51 (d, 2H), 7.48-7.46 (d, 2H), 7.42-7.40 (d, 2H), 7.00-6.95 (d, 2H), 4.01-3.98 (t, 2H), 1.81 (m, 2H), 1.42 (m, 4H), and 0.94 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981120B2
Source datasetuspto-grants-2015_03
ORD IDord-6f320b01a5d04479971267ff11fdb753
Source noteuspto-grants-2015_03