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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84357Generated: October 30, 2026

Pyridine → 1-[5-(1,1'-Biphenyl-4-yl)-pentyl]-pyridinium bromide

https://huagongshe.com/reaction/84357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-(5-Bromopentyl)-1,1'-biphenylHCID 10851940—
Product1-[5-(1,1'-Biphenyl-4-yl)-pentyl]-pyridinium bromideHCID 2478182590%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 4-(5-bromopentyl)-1,1′-biphenyl (335 mg, 1.10 mmol) and pyridine (1 mL) was heated at 60-70° C. for 12 hrs. The resulted mixture was washed with diethyl ether and then dissolved in water (15 mL). The aqueous solution was extracted with diethyl ether (30 mL×3). Water was removed by lyophilization to afford 381 mg of the title compound. Yield: 90%. 1H NMR (300 MHz, CDCl3) δ 1.44 (m, 2H), 1.69 (m, 2H), 2.07 (m, 2H), 2.62 (t, J=7.5 Hz, 2H), 4.96 (t, J=7.5 Hz, 2H), 7.15-7.60 (m, 9H), 8.06 (t, J=6.9 Hz, 2H), 8.42 (d, J=7.8 Hz, 1H), 9.48 (d, J=6.0 Hz, 2H) ppm; 13C NMR (75 MHz, CDCl3) δ 25.6, 30.7, 31.9, 35.2, 61.8, 126.8, 127.0, 127.1, 128.4, 128.8, 128.9, 138.6, 140.8, 141.0, 145.0 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846937B2
Source datasetuspto-grants-2014_09
ORD IDord-a4fa43411a434938907475b98616b05a
Source noteuspto-grants-2014_09