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1394820-99-5

1-((4-(2-fluoro-4-nitrophenoxy)quinolin-7-yl)oxy)-2-Methylpropan-2-ol synthesis

10synthesis methods
4-(2-fluoro-4-nitrophenoxy)quinolin-7-ol

1394820-98-4
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1-((4-(2-fluoro-4-nitrophenoxy)quinolin-7-yl)oxy)-2-Methylpropan-2-ol

1394820-99-5
9 suppliers
inquiry

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Yield:1394820-99-5 42.5%

Reaction Conditions:

with sodium hydroxide in tetrahydrofuran;water at 20 - 45; for 10 h;

Steps:

1.6

Step 6) 1-((4-(2-fluoro-4-nitrophenoxy)quinolin-7-yl)oxy)-2-methylpropan-2-ol To a solution of 4-(2-fluoro-4-nitrophenoxy)quinolin-7-ol (60 g, 0.2 mol) in THF/H2O (1 L, THF/H2O=1:1, v/v) was added NaOH (24 g, 0.6 mol) at room temperature, followed by isobutylene oxide (144 g, 2 mol). The reaction was stirred at 45° C. for 10 hours, and then diluted with EtOAc (1 L). The resulted solution was washed with 1 M NaOH aqueous solution (500 mL*4). The organic layer was separated, dried over Na2SO4 and concentrated in vacuo. The residue was washed with 500 mL of petroleum ether, and collected through filtration to give the title compound as a light yellow solid (31.6 g, 42.5%). MS (ESI, pos. ion) m/z: 373.1 [M+1]; 1H NMR (400 MHz, CDCl3): δ 1.41 (s, 6H), 2.28 (s, 1H), 3.98 (s, 2H), 6.53-6.54 (d, J=5.2 Hz, 1H), 7.26-7.36 (m, 2H), 7.45-7.46 (d, J=2.4 Hz, 1H), 8.12-8.20 (m, 3H), 8.69-8.70 (d, J=4.8 Hz, 1H).

References:

US2012/219522,2012,A1 Location in patent:Page/Page column 21