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Ethanone, 1-(6-fluoro-3-pyridinyl)- (9CI)

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Ethanone, 1-(6-fluoro-3-pyridinyl)- (9CI) Basic information

Product Name:
Ethanone, 1-(6-fluoro-3-pyridinyl)- (9CI)
Synonyms:
  • Ethanone, 1-(6-fluoro-3-pyridinyl)- (9CI)
  • 1-(6-Fluoro-3-pyridinyl)-ethanone
  • 5-Acethyl-2-fluoropyridine
  • 5-Acetyl-2-fluoropyridine
  • 1-(6-Fluoro-3-pyridyl)ethanone
  • Ethanone, 1-(6-fluoro-3-pyridinyl)-
  • 1-(6-Fluoropyridin-3-yl)ethanone 95+%
  • Ethanone, 1-(6-fluoro-3-pyridinyl)- (9CI) ISO 9001:2015 REACH
CAS:
84331-14-6
MF:
C7H6FNO
MW:
139.13
Product Categories:
  • ACETYLGROUP
Mol File:
84331-14-6.mol
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Ethanone, 1-(6-fluoro-3-pyridinyl)- (9CI) Chemical Properties

Boiling point:
246.7±20.0℃ (760 Torr)
Density 
1.175±0.06 g/cm3 (20 ºC 760 Torr)
Flash point:
103.0±21.8℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-2.23±0.10(Predicted)
Appearance
White to light yellow Solid
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Safety Information

HS Code 
2933399990
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Ethanone, 1-(6-fluoro-3-pyridinyl)- (9CI) Usage And Synthesis

Synthesis

774239-06-4

75-16-1

84331-14-6

To a cold solution (-78°C) of 6-fluoro-N-methoxy-N-methylnicotinamide (Method 38, 7.2 g, 39 mmol) in tetrahydrofuran (130 mL) was added slowly and dropwise methylmagnesium bromide (20 mL, 59 mmol, 3 M ether solution). The cooling bath was removed and the reaction mixture was allowed to gradually warm to room temperature with continuous stirring for 2 hours. Upon completion of the reaction, the reaction was quenched with 3 N hydrochloric acid solution and the layers were separated. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 3.8 g of 2-fluoro-5-acetylpyridine in 70% yield. The product was characterized by 1H NMR (CDCl3): δ 8.80 (s, 1H), 8.29-8.43 (m, 1H), 6.98-7.06 (m, 1H), 2.62 (s, 3H).

References

[1] Patent: WO2006/82392, 2006, A1. Location in patent: Page/Page column 116
[2] Patent: US2017/313683, 2017, A1. Location in patent: Paragraph 1251-1252

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