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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Fluoronicotinic acid | HCID 96089 | — |
| Product | 2-Fluoropyridine-3-carbonyl chloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105682B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-980dd44528bf4ed3b8cee5f1bb206c5f |
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| Source note | uspto-grants-2006_09 |
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