2,6-dihydroxy-3-cyanopyridine
2,6-dihydroxy-3-cyanopyridine Basic information
- Product Name:
- 2,6-dihydroxy-3-cyanopyridine
- Synonyms:
-
- 2,6-dihydroxy-3-cyanopyridine
- 3-Pyridinecarbonitrile, 1,2-dihydro-6-hydroxy-2-oxo-
- 1,2-Dihydro-6-hydroxy-2-oxo-3-pyridinecarbonitrile
- 2-hydroxy-6-oxo-1,6-dihydropyridine-3-carbonitrile
- 2,6-dihydroxynicotinonitrile
- 2-hydroxy-6-oxo-1H-pyridine-3-carbonitrile
- 2,6-dihydroxy-3-cyanopyridine ISO 9001:2015 REACH
- 6-Hydroxy-2-oxo-1,2-dihydropyridine-3-carbonitrile
- CAS:
- 35441-10-2
- MF:
- C6H4N2O2
- MW:
- 136.11
- Mol File:
- 35441-10-2.mol
2,6-dihydroxy-3-cyanopyridine Chemical Properties
- Melting point:
- 255 °C(Solv: ethanol (64-17-5))
- Boiling point:
- 349.9±42.0 °C(Predicted)
- Density
- 1.47±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- 3.51±0.58(Predicted)
- Appearance
- Light yellow to yellow Solid
2,6-dihydroxy-3-cyanopyridine Usage And Synthesis
Synthesis
91467-46-8
35441-10-2
In a 2000 L reaction flask, 160 g of 1,3-dibenzyluracil, 55.2 g of cyanoacetamide (1.2 eq.) and sodium methanol were added. Subsequently 2556.6 g (2.5 eq.) of liquid and 800 mL of methanol were added and stirring was initiated. The temperature of the reaction system was raised to 45-50 °C and the reaction was maintained at this temperature for 6 hours. The progress of the reaction was monitored by TLC and after confirming the completion of the reaction, the reaction solution was cooled to 20-30 °C, filtered and the filter cake was washed with 100 mL of methanol. The filter cake was transferred to a 2000 L reaction flask along with 800 g of water. After heating to 70-75 °C, the reaction solution was slowly cooled to 0-5 °C and kept at this temperature for 2 h. Subsequently, filtration was performed and the filter cake was washed with an appropriate amount of ice water to obtain 2,6-dihydroxynicotinonitrile monosodium salt dihydrate. The temperature was controlled at 20-30 °C and the filter cake was slowly added to an aqueous hydrochloric acid solution (prepared from 480 g of water and 66.6 g of concentrated hydrochloric acid). The crystallization was held at 20-30 °C for 1 h. The crystallization was continued to be cooled to 0-5 °C and kept for 2 h. The filtration was withdrawn and the filter cake was washed with an appropriate amount of ice water. After drying, 74.5 g of white solid 3-cyano-2,6-dihydroxypyridine was obtained in 86.5% yield. Its 1H NMR spectrum is shown in Figure 6.
References
[1] Patent: CN108341771, 2018, A. Location in patent: Paragraph 0056-0061
2,6-dihydroxy-3-cyanopyridineSupplier
- Tel
- 001-857-928-2050 or 1-888-588-9418
- sales@chemreagents.com
- Tel
- 021-58099652-8005 13585536065
- bin.wu@shlschem.com
- Tel
- +86057186818502 13588463833
- info@sagechem.com
- Tel
- Mobile:13665161512
- Tel
- +1-510-219-6317
- sales@hbcchem.com
2,6-dihydroxy-3-cyanopyridine(35441-10-2)Related Product Information
- 1,4-Dimethyl-3-cyano-6-hydroxypyrid-2-one
- 1-Ethyl-6-hydroxy-4-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile
- 4-HYDROXY-2,5-DIMETHYL-3-(MORPHOLINOMETHYL)-6-OXO-1,3-CYCLOHEXADIENE-1-CARBONITRILE
- AURORA KA-3873
- N-Butyl-3-cyano-6-hydroxy-4-methyl-2-pyridone
- 1-benzyl-6-hydroxy-4-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile
- SALOR-INT L132802-1EA
- LABOTEST-BB LT00159357
- 6-HYDROXY-2-OXO-4-PHENYL-1,2-DIHYDRO-PYRIDINE-3,5-DICARBONITRILE
- 6-hydroxy-1-(3-methoxypropyl)-4-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile
- 3-Cyano-6-hydroxy-N-(3-isopropoxypropyl)-4-methyl-2-pyridone