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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879141Generated: October 30, 2026

2,6-Difluorophenylboronic acid → HCID 66652899, compound

https://huagongshe.com/reaction/879141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Difluorophenylboronic acidHCID 2734336—
Reactant2-Chloropyrimidine-4-carboxylic acidHCID 22135751—
CatalystHCID 178418807HCID 178418807—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
SolventSodium HydroxideHCID 14798—
ProductHCID 66652899HCID 66652899—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 2-chloropyrimidine-4-carboxylic acid (1.0 equiv.) in DME and 2M Na2CO3 (3:1, 0.25 M) was added 2,6-difluorophenylboronic acid (1.3 equiv.) and Pd(dppf)Cl2-DCM (0.05 equiv.) in a microwave vial. The vial was heated in the microwave at 120° C. for 30 minutes. The mixture was diluted with ethyl acetate and 1N NaOH was added. The organic phase was separated and extracted three more times with 1N NaOH and once with 6N NaOH. The combined aqueous phases were filtered and acidified to pH 1 by the addition of concentrated HCl and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and concentrated to give 2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acid in 81%. LCMS (m/z): 237.0 (MH+), Rt=0.54 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987457B2
Source datasetuspto-grants-2015_03
ORD IDord-dd321826814d4aa4b20b3bd6cbf0b5eb
Source noteuspto-grants-2015_03