HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351286Generated: November 2, 2026
Picolinic acid → Pyridine-2-carbonyl chloride
https://huagongshe.com/reaction/2351286
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Picolinic acid | HCID 1018 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Pyridine-2-carbonyl chloride | HCID 135034 | — |
Reaction Steps
Picolinic acid chloride was prepared by refluxing a solution of picolinic acid (20.0 g, 162 mmol) and thionyl chloride (24.0 mL, 325 mmol) in chloroform (200 mL) overnight. After excess thionyl chloride and chloroform was removed in vacuo, some of the acid chloride (15.0 g, 106 mmol) was added to a solution of 4-cyanoaniline (10.0 g, 84.6 mmol) and triethylamine (30.0 mL, 215 mmol) in methylene chloride (250 mL) at 0° C. under nitrogen. The reaction mixture was stirred at room temperature for 1 hour, poured into water (1 L), basified with 2.5N sodium hydroxide solution, and diluted with methylene chloride. The organic layer was dried over magnesium sulfate and concentrated to give a light brown solid (8.22 g, 36.9 mmol, 44%, mp 156°-159° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04873238 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-7860ae0a220d4a599dafbdc43137eb03 |
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| Source note | uspto-grants-1989_10 |
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