ChemicalBook--->CAS DataBase List--->175596-01-7

175596-01-7

175596-01-7 Structure

175596-01-7 Structure
IdentificationBack Directory
[Name]

4-CYANO-2-FLUOROBENZOIC ACID METHYL ESTER
[CAS]

175596-01-7
[Synonyms]

4-CYANO-2-FLUOROBENZOIC ACID METHYL ESTER
[Molecular Formula]

C9H6FNO2
[MDL Number]

MFCD04335187
[MOL File]

175596-01-7.mol
[Molecular Weight]

179.15
Chemical PropertiesBack Directory
[Boiling point ]

296.0±30.0 °C(Predicted)
[density ]

1.27±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P271-P261-P280
[HS Code ]

2916399090
Spectrum DetailBack Directory
[Spectrum Detail]

4-CYANO-2-FLUOROBENZOIC ACID METHYL ESTER(175596-01-7)1HNMR
4-CYANO-2-FLUOROBENZOIC ACID METHYL ESTER(175596-01-7)19FNMR
Hazard InformationBack Directory
[Synthesis]

4-CYANO-2-FLUOROBENZOIC ACID

164149-28-4

Iodomethane

74-88-4

4-CYANO-2-FLUOROBENZOIC ACID METHYL ESTER

175596-01-7

Step (i) Potassium carbonate (3.70 g, 26.7 mmol) was added to a solution of 4-cyano-2-fluorobenzoic acid (4 g, 24.3 mmol) in N,N-dimethylformamide (DMF, 350 mL). After stirring for 15 min at room temperature, iodomethane (1.66 mL, 26.7 mmol) was slowly added. The reaction vial was sealed and the reaction mixture was stirred at 40 °C for 2 hours. Upon completion of the reaction, most of the DMF was removed by distillation under reduced pressure. the residue was subjected to liquid-liquid partitioning with dichloromethane (DCM, 50 mL) and saturated saline (50 mL). The organic phase was separated and filtered through a short column of silica gel to remove possible solid impurities. Finally, the organic phase was concentrated under reduced pressure to afford methyl 4-cyano-2-fluorobenzoate (4.1 g, 94% yield). Nuclear magnetic resonance hydrogen spectrum (1H NMR, 300 MHz, CDCl3) δ ppm: 3.96 (s, 3H), 7.44-7.48 (m, 1H), 7.49-7.53 (m, 1H), 8.01-8.05 (m, 1H).

[References]

[1] Patent: WO2015/25164, 2015, A1. Location in patent: Page/Page column 81-82
[2] Patent: US2015/57298, 2015, A1. Location in patent: Paragraph 0551
[3] Patent: US2016/207883, 2016, A1. Location in patent: Paragraph 0916-0918
[4] Patent: WO2009/124962, 2009, A2. Location in patent: Page/Page column 141
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