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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288690Generated: October 31, 2026

4-Bromoanisole → 4-(4-Methoxyphenyl)pyridine

https://huagongshe.com/reaction/2288690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanisoleHCID 7730—
Reactant4-Bromopyridinium chlorideHCID 88100—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178491912HCID 178491912—
CatalystBis(triphenylphosphine)nickel(II)chlorideHCID 84306—
SolventTetrahydrofuranHCID 8028—
Solventtert-Butyl methyl etherHCID 15413—
Product4-(4-Methoxyphenyl)pyridineHCID 603813—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A solution of 4-methoxyphenylmagnesium bromide, prepared from 4-bromoanisole (150 g 0.80 mol) and magnesium (20 g, 0.83 mol) in dry tetrahydrofuran (300 mL) is filtered, cooled to -10° C. and added cautiously to a stirred mixture of bis-(triphenylphosphine)nickel (II) chloride (1.5 g, 2.25 mmol) and 4-bromopyridine hydrochloride (65 g, 0.334 mol) in dry tetrahydrofuran (300 mL) at 10° C. under an argon atmosphere. After 50% of the Grignard reagent had been added a vigorous, exothermic reaction sets in and the temperature of the mixture is maintained between 50 and 60° C. throughout the rest of the addition by employing an ice-methanol cooling bath. When the addition is complete the mixture is stirred for 60 min at 50° C. The solvent is evaporated off under reduced pressure to yield a residue which is treated with t-butylmethylether (500 mL) and extracted with hydrochloric acid (3×300 mL of 5M). The combined extracts are washed (t-butylmethylether), basified (aqueous NaOH) and extracted with

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090817
Source datasetuspto-grants-2000_07
ORD IDord-779483bdde874a0a8f42ecd2710f40ed
Source noteuspto-grants-2000_07