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Chemical Structure| 107048-59-9 Chemical Structure| 107048-59-9

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Chemical Structure| 107048-59-9

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Product Details of [ 107048-59-9 ]

CAS No. :107048-59-9
Formula : C12H13BrO3
M.W : 285.13
SMILES Code : O=C(OC)/C(C1=CC=CC=C1CBr)=C/OC

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* 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 [ 107048-59-9 ]

[ 107048-59-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 107048-59-9 ]
  • [ 55690-60-3 ]
  • [ 1070975-53-9 ]
YieldReaction ConditionsOperation in experiment
80.5% To 350 mL of an aqueous solution having 8.0 g of sodium hydroxide, 31.8 g of Intermediate (II) was added and stirred for 20 min. Subsequently, 70 mL of N, N-dimethylformamide (DMF) solution having 54 g of Intermediate (III) was added. The mixture was stirred at room temperature for 6 hrs and water added until the total volume was 1000 mL. The solution was extracted with dichloromethane, dried over anhydrous sodium sulfate, and the product purified by chromatography over silica gel eluted with ethyl acetate/hexane, 52.1 g of a yellow solid was obtained with a total yield was 80.5%. m.p. 85-87 C. 1H NMR (400 MHz, CDCl3) δ: 3.72 (s, 3H, COOCH3), 3.82 (s, 3H, CH-OCH3), 3.84 (s, 3H, OCH3), 4.52 (s, 1H, CH2), 6.94 (dd, J=2.4 Hz, J=8.8 Hz, 1H, ArH), 7.16 (t, J=4.6 Hz, 1H, ArH), 7.29-7.31 (m, 2H, ArH), 7.40 (d, J=2.8 Hz, 1H, ArH), 7.54-7.61 (m, 3H, CH-OCH3, ArH). EI MS: m/z (%) 401 (M+, 4), 369(19), 205 (11), 167 (24), 144 (100), 101 (37). Anal. Calcd for C20H19NO4S2: C, 59.83; H, 4.77; N, 3.49. Found: C, 59.89; H, 5.01; N, 3.27.
80.5% To 350 mL of an aqueous solution having 8.0 g of sodium hydroxide, 31.8 g of Intermediate (II) was added and stirred for 20 min. Subsequently, 70 mL of N, N-dimethylformamide (DMF) solution having 54 g of Intermediate (III) was added. The mixture was stirred at room temperature for 6 hrs and water added until the total volume was 1000 mL. The solution was extracted with dichloromethane, dried over anhydrous sodium sulfate, and the product purified by chromatography over silica gel eluted with ethyl acetate/hexane, 52.1 g of a yellow solid was obtained with a total yield was 80.5%. m.p. 85-87C. 1H NMR (400 MHz, CDCl3) δ: 3.72 (s, 3H, COOCH3), 3.82 (s,3H,=CH-OCH3), 3.84(s, 3H, OCH3), 4.52 (s, 1H, CH2), 6.94 (dd, J = 2.4 Hz, J = 8.8 Hz,1H, ArH),7.16 (t, J = 4.6 Hz, 1H, ArH), 7.29-7.31 (m, 2H, ArH), 7.40 (d, J = 2.8Hz, 1H, ArH), 7.54-7.61 (m,3H, =CH-OCH3, ArH). EI MS: m/z (%) 401 (M+, 4), 369(19), 205 (11), 167 (24), 144 (100), 101 (37). Anal. Calcd for C20H19NO4S2: C, 59.83; H, 4.77; N, 3.49; Found: C, 59.89; H, 5.01; N, 3.27.
 

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