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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917457Generated: November 1, 2026

Sodium Carbonate → 2-Phenylpyridin-4-amine

https://huagongshe.com/reaction/917457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-Chloropyridin-4-amineHCID 84432—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2-Phenylpyridin-4-amineHCID 276283387.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 16.0 g (124 mmol) 2-chloro-4-aminopyridine in 200 ml toluene were added 18.2 g (149 mmol) phenylboronic acid, 7.19 g (6.22 mmol) tetrakis(triphenylphosphine)palladium(0) and 130 ml (260 mmol) 2 M aq. sodium carbonate solution. The mixture was heated at 100° C. for 16 h and then cooled to room temperature and extracted three times with ethyl acetate. The combined organic phases were extracted three times with 200 ml 1 M aq. hydrochloric acid. The combined acid extracts were then made alkaline by addition of 5 M aq. sodium hydroxide solution and extracted three times with dichloromethane. The combined organic extracts were dried over sodium sulfate, and concentrated in vacuo. Flash chromatography (acetone) followed by trituration in hexane containing a little ether afforded 18.5 g (87%) 2-phenyl-pyridin-4-ylamine as a white solid. ES-MS m/e (%): 171 (M+H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273865B2
Source datasetuspto-grants-2007_09
ORD IDord-3f93ae24f3ed46d3b614cd18c8ec8f49
Source noteuspto-grants-2007_09