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CAS No. : | 243128-37-2 | MDL No. : | MFCD01569371 |
Formula : | C8H6FNO | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | FOWHAPVFVBXMBK-UHFFFAOYSA-N |
M.W : | 151.14 | Pubchem ID : | 2737365 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P301+P312-P302+P352-P304+P340-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
100% | With hydrogen; acetic acid;palladium 10% on activated carbon; under 3112.81 Torr; for 8h; | Preparation 98; 4-Fluoro-3-methoxy-benz lamine; Add 4-fluoro-3-methoxy-benzonitrile (2 g, 0. 01 mol), 10% palladium on carbon (0.400 g) and glacial acetic acid (120 ml) to a pressure vessel. Purge the reaction vessel with nitrogen, purge the reaction vessel with hydrogen, pressurize the reaction mixture with hydrogen (415 Kpa), seal the vessel, and agitate the reaction. After 8 hours stop the agitation, vent the excess hydrogen from the vessel and purge the vessel with nitrogen. Filter the reaction mixture to remove the 5% palladium on carbon and return the filtrate for product isolation. Concentrate the crude solution, re-dissolve in CH2C12 (80mL) and washe with 5N NaOH (35mL). Separate the organic and aqueous phases and extract the aqueous with additional CHUCK (20mL). Combine the organic solutions, dry, filter and concentrate to give the crude material 2. 08g (100%). The title compound as the major product (Rf = 0.12, 10% MeOH/CH2C12) is used without further purification. MS (ES+) 156.1 (M+1) +. lH NMR (400MHz, CDC13) : 8 7. 01 (dd, 1H, J= 8.2, 11.4), 6.95 (dd, 1H, J = 2. 1,8. 4), 6.80 (m, 1H), 3.89 (s, 3H), 3.82 (s, 2H), 1.54 (br s, 2H). |
86% | A flame dried 50 mL round bottom flask was charged with lithium aluminum hydride (0.63 g, 16.6 mmol) and to this was added tetrahydrofuran (25 mL). The solution was cooled to 0 0C and 3-methoxy-4-fluorobenzonitrile (1.0 g, 6.62 mmol) was added in one portion. The ice bath was removed after an hour and the resulting mixture was stirred for 16 h after which it was cooled to 0 0C and quenched by adding 0.63 mL water, 0.63 mL 15% NaOH and 1.89 mL water drop- wise and in succession. The mixture was stirred for 20 min and filtered. The filtrate was concentrated in vacuo to obtain 890 mg (86%) of the title compound as an oil. NMR indicated no further purification was required. 1H NMR (300 MHz, DMSO-fife): δ 7.1 (m, 2H), 6.85 (m, IH), 3.84 (s, 3H), 3.7 (s, 2H). 13C NMR (75 MHz, DMSO-^6): δ 150.0 (d, J = 240 Hz), 146.6 (d, J = 10.5 Hz), 141.1 (d, J = 3.75 Hz), 118.75 (d, J = 6.75 Hz), 115.1 (d, J = 18 Hz), 112.5, 55.75, 45.2. HRMS: Calc'd for C8Hi0FNO (M + H): 156.0819; Found: 156.0818 |
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