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Chemical Structure| 192819-46-8 Chemical Structure| 192819-46-8

Structure of 192819-46-8

Chemical Structure| 192819-46-8

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Product Details of [ 192819-46-8 ]

CAS No. :192819-46-8
Formula : C8H11FN2
M.W : 154.19
SMILES Code : NC1=CC(N(C)C)=CC=C1F
MDL No. :MFCD11916053

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Application In Synthesis of [ 192819-46-8 ]

* 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.

  • Downstream synthetic route of [ 192819-46-8 ]

[ 192819-46-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 18542-98-8 ]
  • [ 192819-46-8 ]
YieldReaction ConditionsOperation in experiment
With hydrogen;palladium 10% on activated carbon; In methanol; at 20 - 25℃; under 3750.38 Torr; for 0.5h; 3.23 g (17.54 mmol) of <strong>[18542-98-8](4-fluoro-3-nitrophenyl)-dimethylamine</strong> are added, at a temperature in the region of 20 C., to a suspension of 0.6 g (5.63 mmol) of 10% palladium-on-charcoal in 100 cm3 of methanol. After hydrogenation for 30 minutes in an autoclave under 5 bar of hydrogen, at a temperature in the, region of 25 C., the reaction mixture is filtered, the catalyst is rinsed with 3 times 10 cm3 of methanol, and the filtrate is then concentrated to dryness under reduced pressure (2.7 kPa), to give 2.7 g of 4-fluoro-N1,N1-dimethylbenzene-1,3-diamine, in the form of a brown oil; MS-EI: m/z=154(+)=(M)(+).
With palladium 10% on activated carbon; hydrogen; In methanol; ethyl acetate; for 5.0h; General procedure: Compound 20 (1.00 g, 5 mmol) underwent hydrogenation in the solution of EtOAc (10 ml) and MeOH (10 ml) at H2 atmosphere for 5 h using Pd/C (0.10 g, 10%) as the catalyst. The reaction was then filtered and the solvent was removed in vacuo to afford the compound 21 (0.81 g, 96%).
 

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