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Ethanone, 1-(3-hydroxy-2-pyridinyl)- (9CI)

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Ethanone, 1-(3-hydroxy-2-pyridinyl)- (9CI) manufacturers

Ethanone, 1-(3-hydroxy-2-pyridinyl)- (9CI) Basic information
Product Name:Ethanone, 1-(3-hydroxy-2-pyridinyl)- (9CI)
Synonyms:Ethanone, 1-(3-hydroxy-2-pyridinyl)- (9CI);2-Acetyl-3-hydroxypyridine;Ethanone, 1-(3-hydroxy-2-pyridinyl)-;1-(3-hydroxy-2-pyridinyl)- (9CI);1-(3-hydroxypyridin-2-yl)ethan-1-one;1-(3-hydroxy-2-pyridyl)ethanone;Ethanone, 1-(3-hydroxy-2-pyridinyl)- (9CI) ISO 9001:2015 REACH
CAS:13210-29-2
MF:C7H7NO2
MW:137.14
EINECS:
Product Categories:ACETYLGROUP
Mol File:13210-29-2.mol
Ethanone, 1-(3-hydroxy-2-pyridinyl)- (9CI) Structure
Ethanone, 1-(3-hydroxy-2-pyridinyl)- (9CI) Chemical Properties
Boiling point 311.5±22.0 °C(Predicted)
density 1.217
storage temp. Inert atmosphere,Room Temperature
pka5.76±0.10(Predicted)
AppearanceLight yellow to light brown Solid
Safety Information
HS Code 2933399990
MSDS Information
Ethanone, 1-(3-hydroxy-2-pyridinyl)- (9CI) Usage And Synthesis
Synthesis
Methylmagnesium Bromide

75-16-1

2-CYANO-3-HYDROXYPYRIDINE

932-35-4

Ethanone, 1-(3-hydroxy-2-pyridinyl)- (9CI)

13210-29-2

General procedure for the synthesis of 1-(3-hydroxypyridin-2-yl)ethanone from methylmagnesium bromide and 2-cyano-3-hydroxypyridine: Referring to the method of Example 58, to a solution of tetrahydrofuran (THF, 50 mL) of 2-cyano-3-hydroxypyridine (3.00 g, 25.0 mmol) was added slowly, under cooling in an ice bath, a THF solution of 3M methylmagnesium bromide ( 25 mL). After addition, the reaction mixture was stirred at room temperature for 30 min. Subsequently, the reaction mixture was neutralized with 6N hydrochloric acid solution and extracted twice with ethyl acetate. The organic layers were combined, washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure to afford the title compound 1-(3-hydroxypyridin-2-yl)ethanone (3.43 g, quantitative yield) as a powdered solid. The crude product was used directly in the subsequent reaction without further purification.

References[1] Patent: EP2123652, 2009, A1. Location in patent: Page/Page column 63
[2] Patent: US2017/145026, 2017, A1. Location in patent: Paragraph 0622; 0623
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