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Chemical Structure| 340265-92-1 Chemical Structure| 340265-92-1

Structure of 340265-92-1

Chemical Structure| 340265-92-1

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Product Details of [ 340265-92-1 ]

CAS No. :340265-92-1
Formula : C19H23NO8
M.W : 393.39
SMILES Code : O=C(OCC)C(C(C)=O)C(C1=CC=C([N+]([O-])=O)C=C1)C(C(C)=O)C(OCC)=O
MDL No. :MFCD00351433

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Application In Synthesis of [ 340265-92-1 ]

* 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 [ 340265-92-1 ]

[ 340265-92-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 340265-92-1 ]
  • [ 92289-14-0 ]
YieldReaction ConditionsOperation in experiment
60% With sodium hydroxide; In water; for 3h;Reflux; Compound 4 (45 mmol) was dissolved in a mixture of distilled water (67.5 mL) and sodium hydroxide (67.5 g). The resulting mixture was refluxed vigorously for 3 h, and then cooled to room temperature and poured into water (340 mL). The resulting mixture was extracted with ether (2x100 mL). The water phase was acidified with concentrated hydrochloric acid (190 mL). The precipitated glutaric acid was removed by filtration and washed with cold water to remove sodium chloride. The acid was recrystallized from water and dried in vacuum to give a pale brown solid (6.84 g), 60% yield, mp 236-237 C. 1H NMR (400 MHz, CDCl3) δ/ppm: 12.20 (s, 2H), 8.15 (d, J=6.9 Hz, 2H), 7.57 (d, J=6.9 Hz, 2H), 3.60-3.50 (m, 1H), 2.73 (dd, J=8.1-8.1 Hz, 2H), 2.60 (dd, J=8.1-8.1 Hz, 2H); 13C NMR (100 MHz, CDCl3) δ/ppm: 172.9, 152.1, 146.6, 129.4, 123.7, 39.9, 38.3; FTIR (cm-1): 3209, 2983, 2933, 2907, 1696, 1607, 1515, 1402, 1347, 1311, 1286, 1250, 1220, 1186, 1162, 1118, 884, 862, 849, 753, 698. Anal. Calcd for C11H11NO6: C, 52.18; H, 4.38; N, 5.53. Found: C, 52.16; H, 4.40; N, 5.57.
60% With water; sodium hydroxide; at 100℃; for 3h; Compound 4 (45 mmol) was dissolved in a mixture of distilled water (67.5 mL) and sodium hydroxide (67.5 g). The resulting mixture was refluxed vigorously for 3 h, and then cooled to room temperature and poured into water (340 mL). The resulting mixture was extracted with ether (2x100 mL). The water phase was acidified with concentrated hydrochloric acid (190 mL). The precipitated glutaric acid was removed by filtration and washed with cold water to remove sodium chloride. The acid was recrystallized from water and dried in vacuum to give a pale brown solid (6.84 g), 60% yield, mp 236-237 C .1H NMR (400 MHz, CDCl3) d/ppm: 12.20 (s, 2H), 8.15 (d, J6.9 Hz,2H), 7.57 (d, J6.9 Hz, 2H), 3.60e3.50 (m,1H), 2.73 (dd, J8.1e8.1 Hz,2H), 2.60 (dd, J8.1e8.1 Hz, 2H); 13C NMR (100 MHz, CDCl3) d/ppm:172.9, 152.1, 146.6, 129.4, 123.7, 39.9, 38.3; FTIR (cm1): 3209, 2983,2933, 2907,1696,1607,1515,1402,1347,1311,1286,1250,1220,1186,1162, 1118, 884, 862, 849, 753, 698. Anal. Calcd for C11H11NO6: C,52.18; H, 4.38; N, 5.53. Found: C, 52.16; H, 4.40; N, 5.57.
 

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