| Identification | Back Directory | [Name]
4-Chloropyridine-3-carboxaldehyde | [CAS]
114077-82-6 | [Synonyms]
4-Chloronicotinaldehyde
4-CHLORO-3-FORMYLPYRIDINE
4-chloro-3-pyridylazaldehyde
4-chloropyridin-3-carbaldehyde
4-chloro-3-pyridinecarbaldehyde
4-chloropyridine-3-carbaldehyde
4-chloro-3-pyridincarboxaldehyde
4-CHLOROPYRIDINE-3-CARBOXALDEHYDE
4-Chloro-3-pyridinecarboxaldehyde
4-Chhloropyridine-3-carboxaldehyde
3-Pyridinecarboxaldehyde, 4-chloro-
3-Pyridinecarboxaldehyde,4-chloro-(9CI)
4-Chloropyridine-3-carboxaldehyde≥ 98.5% (HPLC)
4-Chloropyridine-3-carboxaldehyde ISO 9001：2015 REACH
4-Chloro-pyridine-3-carbaldehyde/4- Chloronicotinaldehyde
4-Chloropyridine-3-carboxaldehyde, 4-Chloro-3-formylpyridine | [Molecular Formula]
C6H4ClNO | [MDL Number]
MFCD04112523 | [MOL File]
114077-82-6.mol | [Molecular Weight]
141.56 |
| Chemical Properties | Back Directory | [Boiling point ]
228.8±20.0 °C(Predicted) | [density ]
1.332±0.06 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [form ]
solid | [pka]
1.89±0.10(Predicted) | [color ]
Pale yellow | [InChI]
InChI=1S/C6H4ClNO/c7-6-1-2-8-3-5(6)4-9/h1-4H | [InChIKey]
DYRMBQRXOMOMNW-UHFFFAOYSA-N | [SMILES]
C1=NC=CC(Cl)=C1C=O |
| Hazard Information | Back Directory | [Chemical Properties]
White to light yellow powder | [Synthesis]
General procedure: a tetrahydrofuran solution (50 ml) of 4-chloropyridine (25.0 g, 0.22 mol) was slowly added dropwise to a solution of diisopropylammonium lithium prepared from a hexane solution of 1.6 M n-butyllithium (179 ml, 0.29 mol) with diisopropylamine (33.4 g, 0.33 mol) in tetrahydrofuran (300 ml) under the protection of argon gas, keeping the reaction temperature at -78°C. After dropwise addition, stirring was continued for 30 min. Subsequently, N,N-dimethylformamide (DMF, 19.3 g, 0.26 mol) was added and the reaction mixture was gradually warmed up to room temperature. After completion of the reaction, extraction was carried out with ethyl acetate (200 ml) and 5% aqueous ammonium chloride solution (300 ml). The organic layer was separated, dried with anhydrous magnesium sulfate and concentrated under reduced pressure to remove the solvent to give the crude product 4-chloro-3-pyridinecarboxaldehyde (27 g, 86% yield) as an oil. The product was characterized by 1H-NMR (200 MHz, CDCl3): δ 7.45 (1H, d, J = 5.0 Hz), 8.69 (1H, d, J = 5.0 Hz), 9.05 (1H, s), 10.51 (1H, s). | [References]
[1] Patent: EP1348706, 2003, A1. Location in patent: Page/Page column 37
[2] Patent: US2011/53975, 2011, A1. Location in patent: Page/Page column 60
[3] Journal of the American Chemical Society, 2013, vol. 135, # 40, p. 14916 - 14919
[4] Patent: WO2018/152329, 2018, A1. Location in patent: Page/Page column 44
[5] Patent: WO2004/41806, 2004, A2. Location in patent: Page 88-89 |
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