3-Fluoropyridine-4-carboxylic acid
3-Fluoropyridine-4-carboxylic acid Basic information
- Product Name:
- 3-Fluoropyridine-4-carboxylic acid
- Synonyms:
-
- 3-FLUOROPYRIDINE-4-CARBOXYLIC ACID
- 3-FLUOROISONICOTINIC ACID
- 3-FLUORO-4-PYRIDINECARBOXYLIC ACID
- 3-Fluoropyridine-4-carboxylic acid mono hydrate
- 3-Fluoroisonicotinic
- 3-FLUORONICOTINIC ACID
- 3-FLUOROISONICOTINIC ACID MONO HYDRATE
- 3-Fluoro-4-pyridinecarboxylic
- CAS:
- 393-53-3
- MF:
- C6H4FNO2
- MW:
- 141.1
- EINECS:
- 639-266-3
- Product Categories:
-
- Fluorine series
- Morpholines/Thiomorpholines
- Building Blocks
- Fluorinated
- blocks
- Carboxes
- FluoroCompounds
- Pyridines
- Pyridine
- Pyridine series
- Mol File:
- 393-53-3.mol
3-Fluoropyridine-4-carboxylic acid Chemical Properties
- Melting point:
- 251-254°C (dec.)
- Boiling point:
- 360.0±22.0 °C(Predicted)
- Density
- 1.419±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- pka
- 2.85±0.10(Predicted)
- form
- solid
- color
- White to off-white
- BRN
- 383678
- InChIKey
- POLXLLIQWDBJMD-UHFFFAOYSA-N
- CAS DataBase Reference
- 393-53-3(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,F
- Risk Statements
- 36/37/38-10
- Safety Statements
- 26-36-16
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 2933399990
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
3-Fluoropyridine-4-carboxylic acid Usage And Synthesis
Synthesis
124-38-9
393-53-3
3-Fluoropyridine (25 g, 257 mmol) was slowly added dropwise to a solution of tetrahydrofuran (600 mL) containing butyl lithium (270 mmol) and diisopropylamine (27.4 g, 271 mmol) at -78 °C. The reaction mixture was stirred continuously at this temperature for 1 hour. Subsequently, crushed dry ice was added to the reaction system and gradually warmed to room temperature over 1 hour. Upon completion of the reaction, the pH of the reaction solution was adjusted to 5 with an aqueous solution of hydrogen chloride and acidified. The resulting precipitate was collected by filtration and dried. The final 3-fluoroisonicotinic acid (25.2 g, 179 mmol, 70% yield) was obtained as colorless crystals.
References
[1] Patent: WO2006/36015, 2006, A2. Location in patent: Page/Page column 121-122
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