4-Fluoro-2-methoxybenzonitrile
4-Fluoro-2-methoxybenzonitrile Basic information
- Product Name:
- 4-Fluoro-2-methoxybenzonitrile
- Synonyms:
-
- 4-FLUORO-2-METHOXYBENZONITRILE
- BUTTPARK 80\07-22
- 4-Fluoro-2-methoxybenzonitril
- Benzonitrile, 4-fluoro-2-methoxy- (9CI)
- 4-Fluoro-o-anisonitrile, 2-Cyano-5-fluoroanisole
- Benzonitrile, 4-fluoro-2-methoxy-
- 4-Fluoro-o-anisonitrile
- CAS:
- 191014-55-8
- MF:
- C8H6FNO
- MW:
- 151.14
- Product Categories:
-
- Fluorine series
- Anisoles, Alkyloxy Compounds & Phenylacetates
- Fluorine Compounds
- Nitriles
- HALIDE
- Aromatic Nitriles
- Mol File:
- 191014-55-8.mol
4-Fluoro-2-methoxybenzonitrile Chemical Properties
- Melting point:
- 75 °C
- Boiling point:
- 239.2±20.0 °C(Predicted)
- Density
- 1.18±0.1 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- form
- crystalline solid
- color
- White to off-white
- CAS DataBase Reference
- 191014-55-8(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 20/21/22-36/37/38
- Safety Statements
- 23-36/37/39
- RIDADR
- 3276
- Hazard Note
- Irritant
- HazardClass
- 6.1
- HS Code
- 2926907090
4-Fluoro-2-methoxybenzonitrile Usage And Synthesis
Chemical Properties
off-white crytalline
Synthesis
450-88-4
544-92-3
191014-55-8
General procedure for the synthesis of 2-methoxy-4-fluorobenzonitrile from 2-bromo-5-fluoroanisole and cuprous cyanide: to a solution of N-methylpyrrolidone (100 mL, Sure Seal; Aldrich) containing 1-bromo-4-fluoro-2-methoxybenzene (9.0 g) was added cuprous cyanide (6.6 g, 73.7 mmol, 1.8 equiv. Aldrich). The reaction mixture was stirred at 180 °C for 5.5 h in an anhydrous nitrogen atmosphere. After completion of the reaction, it was cooled to room temperature, a 14% aqueous ammonia solution (330 mL) was added, and stirring was continued at room temperature for 45 min. The reaction mixture was extracted with ether (100 mL x 3), and the organic phases were combined, washed sequentially with dilute ammonia, dilute hydrochloric acid and brine, and then dried with anhydrous magnesium sulfate, and concentrated to give 2-methoxy-4-fluorobenzonitrile (5.2 g, 85% yield in two steps). The product was a white solid with the following 1H NMR (CDCl3,500MHz) data: δ 3.91 (3H, s, OMe), 6.69 (1H, dd, J = 2.3Hz, J = 10.5Hz, Ar-H), 6.72 (1H, dt, J = 2.5Hz, J = 8.0Hz, Ar-H), 7.55 (1H, dd, J = 6.5 Hz, J = 8.5 Hz, Ar-H); 13C NMR (CDCl3,125.8 Hz) data as follows: δ 56.49, 98.16, 100.06, 100.27, 108.31, 108.50, 115.83, 135.37, 135.46, 163.25, 163.34, 165.47, 167.50. 167.50. analytical samples were obtained by ether milling. Calculated values for elemental analysis (C8H6FNO): C, 63.57; H, 4.00; N, 9.26; measured values: C, 63.36; H, 3.91; N, 9.16.
References
[1] Patent: US2005/267105, 2005, A1. Location in patent: Page/Page column 67
[2] Patent: EP1510516, 2005, A1. Location in patent: Page/Page column 88
[3] Patent: US2007/111984, 2007, A1. Location in patent: Page/Page column 32-33
[4] Patent: US2007/129379, 2007, A1. Location in patent: Page/Page column 26
[5] Patent: WO2007/64316, 2007, A1. Location in patent: Page/Page column 152
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4-Fluoro-2-methoxybenzonitrile(191014-55-8)Related Product Information
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- p-Anisaldehyde
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- 4-FLUORO-2-METHOXYBENZALDEHYDE
- 4-Fluorobenzonitrile
- 5-Fluoro-2-methoxybenzonitrile, 98+%,5-FLUORO-2-METHOXYBENZONITRILE
- 3-FLUORO-5-METHOXYBENZONITRILE,3-Fluoro-5-methoxybenzonitrile 98%,3-Fluoro-5-methoxybenzonitrile98%
- 4-Fluoro-3-methoxybenzonitrile 99%,4-Fluoro-3-methoxybenzonitrile99%,4-FLUORO-3-METHOXYBENZONITRILE
- Fluorine
- 2-FLUORO-6-METHOXYBENZONITRILE
- 2-FLUORO-5-METHOXYBENZONITRILE,2-Fluoro-5-methoxybenzonitrile98%
- 5-FLUORO-2-METHYLANISOLE