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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534730Generated: October 28, 2026

Oxalyl chloride → 6-(4-Fluorophenyl)-2-methyl-3-pyridinecarbonyl chloride

https://huagongshe.com/reaction/534730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant6-(4-Fluorophenyl)-2-methylpyridine-3-carboxylic acidHCID 24277790—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product6-(4-Fluorophenyl)-2-methyl-3-pyridinecarbonyl chlorideHCID 8661810841.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

6-(4-Fluorophenyl)-2-methyl-3-pyridinecarboxylic acid (0.2 g, 0.866 mol) was suspended in DCM (14 mL) and DMF (1 drop) was added. The mixture was cooled in an ice-bath and oxalyl chloride (0.226 mL, 2.598 mmol) was added portion wise over 5 minutes. The mixture was heated to 40° C. for 90 minutes. The mixture was allowed to cool and the solvent removed under vacuum to give 6-(4-fluorophenyl)-2-methyl-3-pyridinecarbonyl chloride as a yellow solid (0.270 g) which was used directly in step 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853218B2
Source datasetuspto-grants-2014_10
ORD IDord-b7ae2b929ab24665b00a7e426d28de59
Source noteuspto-grants-2014_10