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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594219Generated: November 1, 2026

2-Bromopyridine → Methyl 2-chloro-5-(pyridin-2-yl)benzoate

https://huagongshe.com/reaction/594219

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-3-(methoxycarbonyl)benzeneboronic acidHCID 23005334—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-chloro-5-(pyridin-2-yl)benzoateHCID 57422925—

Reaction Steps

A mixture of commercially available 2-bromopyridine (294 mg; 1.86 mmol), 4-chloro-3-(methoxycarbonyl)phenylboronic acid (400 mg; 1.86 mmol), K2CO3 (515 mg; 3.73 mmol), and PdCl2(PPh3)2 (130 mg; 0.18 mmol) in THF (4 ml) and water (4 ml) was stirred at rt, under nitrogen, for 20 h. Water and AcOEt were added. The separated aq. layer was further extracted with AcOEt. The mixed organic layers were washed with brine, dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure. Purification by FC (heptane/AcOEt=7/3) afforded methyl 2-chloro-5-(pyridin-2-yl)benzoate as a colorless solid. LC-MS (conditions A): tR=0.65 min.; [M+H]+: 248.02 g/mol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-d5d8bed17b5b4dfebe86acafc69c115c
Source noteuspto-grants-2016_01