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Chemical Structure| 64393-83-5 Chemical Structure| 64393-83-5

Structure of 64393-83-5

Chemical Structure| 64393-83-5

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Product Details of [ 64393-83-5 ]

CAS No. :64393-83-5
Formula : C10H7FO4
M.W : 210.16
SMILES Code : O=C(O)C(CC(C1=CC=C(F)C=C1)=O)=O

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Application In Synthesis of [ 64393-83-5 ]

* 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 [ 64393-83-5 ]

[ 64393-83-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 31686-94-9 ]
  • [ 64393-83-5 ]
YieldReaction ConditionsOperation in experiment
64% With sodium hydroxide; In tetrahydrofuran; water; at 20℃; for 0.25h; To a solution of 2b (3.38 g, 14.2 mmol) in THF (47 mL) was added a solution of NaOH (5.68 g, 142 mmol) in 45 mL of water. The reaction stirred at room temperature for 15 min., then the organic solvent was removed by rotary evaporation. The aqueous phase was extracted with Et2O (3 350 mL), then acidified with conc. HCl. The aqueouslayer was extracted with EtOAc (3 3 100 mL), and the combined organic layers were washed with brine (50 mL), dried over Na2SO4,filtered, and concentrated to obtain 3b (1.92 g, 64% yield) as an off-white solid. 1H NMR (500 MHz, CDCl3) d 15.21 (s, 1H), 8.25 - 8.01(m, 2H), 7.27 (s, 1H), 7.22 (t, J = 8.6 Hz, 2H), 7.14 (s, 1H). 1H NMR (500 MHz, DMSO-D6) d 8.30 - 8.02 (m, 2H), 7.41 (t, J = 8.8 Hz, 2H), 7.10 (s, 1H), (Carboxylic acid -OH and enol-OH not observed). 13C NMR (125 MHz, CDCl3) d 185.90, 174.19, 166.49 (d, J = 257.7 Hz),161.63, 130.62 (d, J = 9.5 Hz)*, 129.42 (d, J = 3.1 Hz), 116.44 (d, J = 22.1 Hz)*, 95.08. * Indicates two equivalent carbons with the samechemical shift that couple with 19F.
64% With water; sodium hydroxide; In tetrahydrofuran; at 20℃; for 0.25h; To a solution of 2b (3.38 g, 14.2 mmol) in THF (47 mL) was added a solution of NaOH (5.68 g, 142 mmol) in 45 mL of water. The reaction stirred at room temperature for 15 min., then the organic solvent was removed by rotary evaporation. The aqueous phase was extracted with Et20 (3 x 50 mL), then acidified with cone. HC1. The aqueous layer was extracted with EtOAc (3 x 100 mL), and the combined organic layers were washed with brine (50 mL), dried over Na2S04, filtered, and concentrated to obtain 3b (1.92 g, 64% yield) as an off-white solid. NMR (500 MHz, CDCl3) d 15.21 (s, 1H), 8.25 - 8.01 (m, 2H), 7.27 (s, 1H), 7.22 (t, J = 8.6 Hz, 2H), 7.14 8.30 - 8.02 (m, 2H), 7.41 (t, J = 8.8 Hz, 2H), 7.10 (s, 1H), (Carboxylic acid -OH and enol-OH not observed). 13C NMR (125 MHz, CDCl3) d 185.90, 174.19, 166.49 (d, J = 257.7 Hz), 161.63, 130.62 (d, J = 9.5 Hz)*, 129.42 (d, J = 3.1 Hz), 116.44 (d, J = 22.1 Hz)*, 95.08. * Indicates two equivalent carbons with the same chemical shift that couple with 19F.
 

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