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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848604Generated: October 30, 2026

Sodium Carbonate → 4-Chloro-3-(3,5-dichloro-pyridin-2-yl)-benzoic acid methyl ester

https://huagongshe.com/reaction/1848604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromo-3,5-dichloropyridineHCID 817090—
ReactantMethyl 4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoateHCID 20816364—
CatalystHCID 178418397HCID 178418397—
SolventToluene ethanolHCID 21863594—
Product4-Chloro-3-(3,5-dichloro-pyridin-2-yl)-benzoic acid methyl esterHCID 6860212294.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2-bromo-3,5-dichloropyridine (2.72 g, 12 mmol), 4-chloro-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzoic acid methyl ester (1.78 g, 6 mmol)), 2N Na2CO3 (9.0 mL, 18 mmol), Pd(PPh3)4 (0.35 g, 0.3 mmol) in toluene/ethanol (30 mL/6 mL) was sealed and heated at 90° C. for 12 hrs. The mixture was concentrated and partitioned between ethyl acetate and water. The ethyl acetate layer was washed with water and brine and was dried over MgSO4. After filtration and concentration, purification by silica gel chromatography eluting with ethyl acetate/hexane (5/95) gave 4-chloro-3-(3,5-dichloro-pyridin-2-yl)-benzoic acid methyl ester (1.8 g). MS (M+H)+: 315.6, tR=8.505 min (method 2)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952161B2
Source datasetuspto-grants-2015_02
ORD IDord-0d2ad26c0fc54432b13a521755abfe98
Source noteuspto-grants-2015_02