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Chemical Structure| 1190075-01-4 Chemical Structure| 1190075-01-4

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Chemical Structure| 1190075-01-4

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Product Details of [ 1190075-01-4 ]

CAS No. :1190075-01-4
Formula : C8H10FNO
M.W : 155.17
SMILES Code : NC1=CC(OCC)=CC=C1F
MDL No. :MFCD18205032

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Application In Synthesis of [ 1190075-01-4 ]

* 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 [ 1190075-01-4 ]

[ 1190075-01-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 900174-60-9 ]
  • [ 1190075-01-4 ]
YieldReaction ConditionsOperation in experiment
48% With copper(I) oxide; ammonium hydroxide; In methanol; water; for 7h; [00300j 43E. 5-Ethoxy-2-fluoroaniline: To a solution of (5-ethoxy-2- fluorophenyl)boronic acid (10.1 g, 55.0 mmol) in MeOH (220 mL) was added 14.8 M aq.NH4OH (18.6 mL, 275 mmol) and cuprous oxide (1.57 g, 11.0 mmol). The reaction mixture was stirred under air for 7 h. The reaction mixture was concentrated. The crude product was dissolved in EtOAc/hexanes (2:1). The material was filtered through CELITE and concentrated. The crude material was purified by silica chromatography to provide 43E (4.10 g, 26.4 mmol, 48% yield) as a brown oil. LC-MS Anal. Calc’d for C8H20FNO: 155.17, found [M+H] 156.1. ‘HNMR(400 MHz, CDC13) ö 6.86 (dd,J=10.9, 8.8 Hz, 1H), 6.32 (dd, J=7.5, 2.9 Hz, 1H), 6.20 (dt, J=8.8, 3.3 Hz, 1H), 3.94 (q, J=6.9 Hz, 2H), 3.68 (br. s, 2H), 1.37 (t, J=6.9 Hz, 3H).
48% With copper(I) oxide; ammonium hydroxide; In methanol; water; for 7h; 29A. 5-Ethoxy-2-fluoroaniline To a solution of (5-ethoxy-2-fluorophenyl)boronic acid (10.1 g, 55.0 mmol) in MeOH (220 mL) was added 14.8 M aqueous NH4OH (18.6 mL, 275 mmol), and then cuprous oxide (1.57 g, 11.0 mmol). The reaction mixture was stirred under air for 7 h. The reaction mixture was concentrated. The crude material was dissolved in EtOAc/Hex (2:1). The material was filtered through CELITE and concentrated. The crude material was purified by flash chromatography to provide 5-ethoxy-2-fluoroaniline (4.10 g, 26.4 mmol, 48% yield) as a brown oil. LC-MS Anal. Calc'd for C8H20FNO 155.17. found [M+H] 156.1. 1H NMR (400 MHz, CDCl3) δ 6.86 (dd, J=10.9, 8.8 Hz, 1H), 6.32 (dd, J=7.5, 2.9 Hz, 1H), 6.20 (dt, J=8.8, 3.3 Hz, 1H), 3.94 (q, J=6.9 Hz, 2H), 3.68 (br. s., 2H), 1.37 (t, J=6.9 Hz, 3H).
48% With copper(I) oxide; ammonium hydroxide; In methanol; for 7h; To a solution of (5-ethoxy-2-fluorophenyl) boronic acid (10.1 g, 55.0 mmol) in MeOH (220 mL) was added 14.8 M aq. NH4OH (18.6 mL, 275 mmol) and then cuprous oxide (1.57 g, 11.0 mmol). The reaction mixture was stirred under air for 7 h. The reaction mixture was concentrated. The crude product was dissolved in EtOAc/hexanes (2: 1). The material was filtered through CELITE and concentrated. The crude material was purified by silica chromatography to provide 9A (4.10 g, 26.4 mmol, 48% yield) as a brown oil. LC-MS Anal. Calc'd for C8Hi0FNO: 155.17, found [M+H] 156.1. 1H NMR (400 MHz, CDC13) δ 6.86 (dd, J=10.9, 8.8 Hz, IH), 6.32 (dd, J=7.5, 2.9 Hz, IH), 6.20 (dt, J=8.8, 3.3 Hz, IH), 3.94 (q, J=6.9 Hz, 2H), 3.68 (br. s, 2H), 1.37 (t, J=6.9 Hz, 3H).
 

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