ChemicalBook > Product Catalog > Pharmaceutical intermediates > Heterocyclic compound > Pyridine compound > Chloropyridine > 6-CHLORO-PYRIDINE-2-CARBONYL CHLORIDE
6-CHLORO-PYRIDINE-2-CARBONYL CHLORIDE
6-CHLORO-PYRIDINE-2-CARBONYL CHLORIDE Basic information
- Product Name:
- 6-CHLORO-PYRIDINE-2-CARBONYL CHLORIDE
- Synonyms:
-
- 6-CHLORO-PYRIDINE-2-CARBONYL CHLORIDE
- 2-Pyridinecarbonyl chloride, 6-chloro- (9CI)
- 6-chloropicolinoyl chloride
- 6-Chloro-2-pyridinecarbonyl chloride
- 6-Chloropicolinic acid chloride
- 2-Pyridinecarbonylchloride, 6-chloro-
- 6-CHLORO-PYRIDINE-2-CARBONYL CHLORIDE ISO 9001:2015 REACH
- 2-Chloro-6-pyridylcarbonyl chloride
- CAS:
- 80099-98-5
- MF:
- C6H3Cl2NO
- MW:
- 176
- Product Categories:
-
- ACIDHALIDE
- Mol File:
- 80099-98-5.mol
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6-CHLORO-PYRIDINE-2-CARBONYL CHLORIDE Chemical Properties
- Boiling point:
- 239.0±20.0 °C(Predicted)
- Density
- 1.454±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- -2.22±0.10(Predicted)
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6-CHLORO-PYRIDINE-2-CARBONYL CHLORIDE Usage And Synthesis
Synthesis
19621-92-2
80099-98-5
General procedure for the synthesis of 6-chloropyridinecarbonyl chloride from 6-hydroxypyridine-2-carboxylic acid: to 20 g (144 mmol) of 6-hydroxypyridine-2-carboxylic acid was added 50.6 g (330 mmol) of phosphorus trichloride and 99.8 g (479 mmol) of phosphorus pentachloride, and the reaction was carried out by stirring the mixture for 8 hours at 90 °C. Upon completion of the reaction, the mixture was cooled, followed by the addition of 8.6 g of formic acid, and the reaction mixture was concentrated using a rotary evaporator to quantitatively obtain the target product 6-chloropyridinecarbonyl chloride.
References
[1] Patent: US2004/14977, 2004, A1. Location in patent: Page 20
[2] Patent: EP1302466, 2003, A1
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