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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116636Generated: October 25, 2026

Pyridinium chloride → (4-Bromo-2-hydroxyphenyl)(4-fluorophenyl)methanone

https://huagongshe.com/reaction/2116636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridinium chlorideHCID 10176127—
Reactant(4-Bromo-2-methoxyphenyl)(4-fluorophenyl)methanoneHCID 59814869—
SolventDiethyl EtherHCID 3283—
Product(4-Bromo-2-hydroxyphenyl)(4-fluorophenyl)methanoneHCID 59814864—

Reaction Conditions

Temperature170 °C

Reaction Steps

A mixture of (4-bromo-2-methoxyphenyl)(4-fluorophenyl)methanone (1.60 g, 5.18 mmol) and pyridine hydrochloride (15.0 g, 130 mmol) was heated at 170° C. for 4.5 h and allowed to cool to rt. The resulting mixture was diluted with Et2O and washed with a 2N HCl solution. The ether layer was extracted twice with a 1N NaOH solution. The combined aqueous layers were acidified and extracted with Et2O, and the combined organics dried (MgSO4), filtered and concentrated. The title compound was obtained as a yellow solid, slightly contaminated with an impurity. It was used as such in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439260B2
Source datasetuspto-grants-2008_10
ORD IDord-861ff9e4101d4f1bb3dbfa67fc26ed69
Source noteuspto-grants-2008_10