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