ChemicalBook--->CAS DataBase List--->17228-75-0

17228-75-0

17228-75-0 Structure

17228-75-0 Structure
IdentificationBack Directory
[Name]

2,6-DICHLORO-4-METHOXY-PYRIDINE
[CAS]

17228-75-0
[Synonyms]

4-Methoxy-2,6-dichloropyridine
2,6-DICHLORO-4-METHOXY-PYRIDINE
Pyridine, 2,6-dichloro-4-methoxy-
2,6-Dichloro-4-methoxypyridine 99%
[Molecular Formula]

C6H5Cl2NO
[MDL Number]

MFCD00955755
[MOL File]

17228-75-0.mol
[Molecular Weight]

178.02
Chemical PropertiesBack Directory
[Boiling point ]

255.0±35.0 °C(Predicted)
[density ]

1.363±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

solid
[pka]

-0.91±0.10(Predicted)
[color ]

White to off-white
[InChI]

InChI=1S/C6H5Cl2NO/c1-10-4-2-5(7)9-6(8)3-4/h2-3H,1H3
[InChIKey]

MMQWWYZZOZBFHY-UHFFFAOYSA-N
[SMILES]

C1(Cl)=NC(Cl)=CC(OC)=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P301+P312-P305+P351+P338
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

2,6-DICHLORO-4-METHOXY-PYRIDINE(17228-75-0)1HNMR
2,6-DICHLORO-4-METHOXY-PYRIDINE(17228-75-0)FT-IR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

2,4,6-Trichloropyridine

16063-69-7

2,6-DICHLORO-4-METHOXY-PYRIDINE

17228-75-0

To a solution of 2,4,6-trichloropyridine (3.64 g, 20.0 mmol) in DMF (20 mL) was slowly added NaH (60% dispersed in mineral oil, 840 mg, 21 mmol) and methanol (673 mg, 21 mmol) at 0 °C. The reaction mixture was stirred at room temperature for 16 hours. Upon completion of the reaction, the mixture was concentrated and partitioned between ethyl acetate (30 mL) and water (15 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by silica gel column chromatography to afford 2,6-dichloro-4-methoxypyridine (3.0 g, yield: 94%) using ethyl acetate (0-5%) in hexane as eluent.

[References]

[1] Patent: WO2018/106459, 2018, A1. Location in patent: Paragraph 00110
[2] Bioorganic and Medicinal Chemistry, 2017, vol. 25, # 15, p. 3947 - 3963
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