Computed Tomography 2019
DOI: 10.1007/978-3-030-26957-9_5
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Dose and Risk Characterization in CT

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“…Yield = 90%. 1 H NMR (300 MHz, CDCl 3 ) δ (ppm): 8.64 (2H, dd, J 1 = 12.0 Hz, J 2 = 3.0 Hz), 8.50 (1H, d, J = 6.0 Hz), 7.85 (2H, dd, J 1 = 15.0 Hz, J 2 = 6.0 Hz), 7.55 (1H, s), 7.02 (2H, d, 6 Hz), 4.23 (2H, t, J = 9.0 Hz), 4.08 (2H, t, J = 9.0 Hz), 2.27 (2H, quin, J = 6.0 Hz). 13 was dissolved in acetonitrile, and the corresponding alkyl bromide compound (n-octyl, n-decyl, or n-tetradecyl) was added to the solution and heated to reflux for 72 h (4 days for n-tetradecyl alkyl bromide).…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
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“…Yield = 90%. 1 H NMR (300 MHz, CDCl 3 ) δ (ppm): 8.64 (2H, dd, J 1 = 12.0 Hz, J 2 = 3.0 Hz), 8.50 (1H, d, J = 6.0 Hz), 7.85 (2H, dd, J 1 = 15.0 Hz, J 2 = 6.0 Hz), 7.55 (1H, s), 7.02 (2H, d, 6 Hz), 4.23 (2H, t, J = 9.0 Hz), 4.08 (2H, t, J = 9.0 Hz), 2.27 (2H, quin, J = 6.0 Hz). 13 was dissolved in acetonitrile, and the corresponding alkyl bromide compound (n-octyl, n-decyl, or n-tetradecyl) was added to the solution and heated to reflux for 72 h (4 days for n-tetradecyl alkyl bromide).…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
“…mp = 70−73 °C. 1 H NMR (300 MHz, CDCl 3 ) δ (ppm): 10.56 (1H, s), 8.56 (2H, dd, J 1 = 15.0 Hz, J 2 = 6.0 Hz), 8.42 (1H, d, J = 6.0 Hz), 7.80 (2H, dd, J 1 = 9.0 Hz, J 2 = 6.0 Hz), 7.71 (1H, s), 7.39 (1H, s), 4.52 (2H, t, J = 6.0 Hz), 4.38 (2H, t, J = 6.0 Hz), 4.20 (2H, t, J = 6.0 Hz), 2.44 (2H, quin, J = 6.0 Hz), 1.95, (2H, m), 1. 27 1 H NMR (300 MHz, CDCl 3 ) δ (ppm): 10.52 (1H, s), 8.56 (2H, t, J = 9.0 Hz), 8.41 (1H, d, J = 9.0 Hz), 7.79 (3H, m), 7.44 (1H, s), 4.54 (2H, t, J = 6.5 Hz), 4.40 (2H, t, J = 6.5 Hz), 4.20 (2H, t, J = 6.5 Hz), 2.45 (2H, quin, J = 6.5 Hz), 1.92 (4H, m), 1.24 (14H, m), 0.86 (3H, t, J = 6.0 Hz).…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
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