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2,3-Dichloro-5-hydroxypyridine

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2,3-Dichloro-5-hydroxypyridine Basic information

Product Name:
2,3-Dichloro-5-hydroxypyridine
Synonyms:
  • 2,3-DICHLORO-5-HYDROXYPYRIDINE
  • 5,6-Dichloro-3-hydroxypyridine
  • 3-Pyridinol,5,6-dichloro-
  • 3-Dichloro-5-hydroxypyridine
  • 5,6-dichloro-3-pyridinol
  • 2,3-Dichloro-5-hydroxypyridine ISO 9001:2015 REACH
CAS:
110860-92-9
MF:
C5H3Cl2NO
MW:
163.99
Product Categories:
  • Heterocycle-Pyridine series
  • Boronic Acid
Mol File:
110860-92-9.mol
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2,3-Dichloro-5-hydroxypyridine Chemical Properties

Melting point:
184.0 to 188.0 °C
Boiling point:
365.5±37.0 °C(Predicted)
Density 
1.561±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder to crystal
pka
7.91±0.10(Predicted)
color 
White to Light yellow to Light orange
CAS DataBase Reference
110860-92-9(CAS DataBase Reference)
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Safety Information

HS Code 
2933399990
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2,3-Dichloro-5-hydroxypyridine Usage And Synthesis

Uses

5,6-Dichloropyridin-3-ol is a useful research chemical used in the preparation of bi- or tricyclic heterocycles with sulfur containing substituents as pesticides.

Synthesis

110861-18-2

110860-92-9

General procedure for the synthesis of 2,3-dichloro-5-hydroxypyridine from 5,6-dichloropyridin-3-yl acetate: an aqueous solution (7 mL) of potassium hydroxide (KOH, 728 mg, 13 mmol) was slowly added to an aqueous solution (7 mL) of tetrahydrofuran (THF, 10 mL) of 5,6-dichloropyridin-3-yl acetate (1 g, 4.8 mmol) at 0 °C. After the addition was completed, the reaction mixture was stirred for 2 h at room temperature. Subsequently, the pH of the mixture was adjusted to a weak base with dilute hydrochloric acid and filtered. The filtrate was purified by recrystallization to afford the target product 2,3-dichloro-5-hydroxypyridine (517 mg, yield: 65%). The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6) with chemical shifts δ (ppm) of 7.47 (d, 1H), 7.93 (d, 1H), 10.72 (s, 1H).

References

[1] Synthesis, 1990, # 6, p. 499 - 501
[2] Patent: WO2016/91731, 2016, A1. Location in patent: Page/Page column 140
[3] Patent: US6432880, 2002, B1
[4] Patent: US6133253, 2000, A
[5] Tetrahedron Letters, 2013, vol. 54, # 19, p. 2303 - 2307

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