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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214225Generated: November 2, 2026

Thionyl Chloride → 2-Fluoropyridine-3-carbonyl chloride

https://huagongshe.com/reaction/2214225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-Fluoronicotinic acidHCID 96089—
Product2-Fluoropyridine-3-carbonyl chlorideHCID 21959582—

Reaction Steps

To a solution of 2-fluoropyridine (10 g, 100 mmol) in THF (150 mL) under −78° C. was added an LDA solution (2M in heptane/THF/ethylbenzene, 60 mL) dropwise. The mixture was stirred at −78° C. for 3 h, then was quenched with a stream of dry CO2. After warming to RT, the mixture was partitioned between EtOAc (100 mL) and H2O (200 mL). The aqueous layer was acidified to pH between 3–4, and extracted with EtOAc. The organic solution was collected and washed with brine and dried over Na2SO4. After removing the solvent in vacuum, 2-fluoropyridine-3-carboxylic acid was obtained as a brown oil. MS: 140 (M−H). Calc'd. for C6H4FNO2—141.10. 2-Fluoropyridine-3-carboxylic acid (7 g) was suspended in SOCl2 (100 mL). After heating under reflux for 2 h, the mixture became homogeneous. Access SOCl2 was removed in vacuo to afford a brown solid as desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105682B2
Source datasetuspto-grants-2006_09
ORD IDord-980dd44528bf4ed3b8cee5f1bb206c5f
Source noteuspto-grants-2006_09