ChemicalBook--->CAS DataBase List--->59288-40-3

59288-40-3

59288-40-3 Structure

59288-40-3 Structure
IdentificationBack Directory
[Name]

3-Pyridinecarboxylic acid, 5-hydroxy-6-iodo-, ethyl ester
[CAS]

59288-40-3
[Synonyms]

ethyl 5-hydroxy-6-iodonicotinate
5-Hydroxy-6-iodo-nicotinic acid ethyl ester
5-hydroxy-6-iodo-3-Pyridinecarboxylic acid ethyl ester
3-Pyridinecarboxylic acid, 5-hydroxy-6-iodo-, ethyl ester
[Molecular Formula]

C8H8INO3
[MDL Number]

MFCD13688989
[MOL File]

59288-40-3.mol
[Molecular Weight]

293.06
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

3-Pyridinecarboxylic acid, 5-hydroxy-6-iodo-, ethyl ester(59288-40-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethyl 5-hydroxynicotinate

59288-38-9

3-Pyridinecarboxylic acid, 5-hydroxy-6-iodo-, ethyl ester

59288-40-3

General procedure for the synthesis of ethyl 5-hydroxy-6-iodo-3-pyridinecarboxylate from ethyl 5-hydroxynicotinate: a solution of ethyl 5-hydroxynicotinate was added to water (15 L), followed by sodium carbonate (733 g, 30.7 mol) and iodine (965 g, 15.3 mol). The reaction was carried out at room temperature with stirring for 2 hours. The progress of the reaction was monitored by thin layer chromatography (TLC) (unfolding agent: petroleum ether/ethyl acetate = 1/1, Rf = 0.8) and after confirming the completion of the reaction, the pH was adjusted to 7 by slowly adding 1N hydrochloric acid to the reaction solution, when a solid precipitated. The solid product was collected by filtration and dried under reduced pressure to give ethyl 5-hydroxy-6-iodo-3-pyridinecarboxylate (925 g) as a yellow solid in 82.5% yield.

[References]

[1] Patent: CN105418620, 2016, A. Location in patent: Paragraph 0008; 0032; 0033
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