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Chemical Structure| 6448-14-2 Chemical Structure| 6448-14-2

Structure of 6448-14-2

Chemical Structure| 6448-14-2

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Product Details of [ 6448-14-2 ]

CAS No. :6448-14-2
Formula : C13H16O2
M.W : 204.26
SMILES Code : C=C(C1=CC=C(CC(C)C)C=C1)C(O)=O

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Application In Synthesis of [ 6448-14-2 ]

* 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 [ 6448-14-2 ]

[ 6448-14-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 6448-14-2 ]
  • [ 51146-57-7 ]
YieldReaction ConditionsOperation in experiment
96% In the glove box, the catalyst [(Sa-DTB-SIPHOX)Ir(COD)]BARF 4 (4.7 mg, 0.0025 mmol) and 2 - (4 - isobutyl-phenyl) acrylic acid 5 (102 mg, 0.5 mmol) are weighted in the reaction inner tube with stirring bar, then the reaction inner tube is sealed for use. When the reaction inner tube is took out, triethylamine (25 mg, 0.25 mmol) and anhydrous methanol (2 mL) are added with a syringe, then the inner tube is placed into the hydrogenation reactor, the mixture is stirred at room temperature under the hydrogen pressure of 0.6 Mpa to react for 24 h. Then the stirring is stopped, the hydrogen is released. After the system is condensed by evaporating off rotatably, the system is adjusted pH <3 with 3N hydrochloric acid water solution, extracted with diethyl ether (10 mL .x. 3), and separated, the organic phase is collected, washed with saturated salt water, and dried with anhydrous sodium sulfate. The desiccant is removed by suction filtration, the solvent is evaporated off by rotating, then the object product 6 is obtained, and is a white solid, through the 1H NMR analysis, the conversion rate is 100percent and the yield is 96percent. Mp 53-55 °C; [alpha]30,D -41.5 (c 2.0, ethanol); 1H NMR (400 MHz, CDCl3): delta 11.27 (brs, 1H, COOH), 7.24 (d, J = 8.4 Hz, 2H, Ar-H), 7.08 (d, J = 7.6 Hz, 2H, Ar-H), 3.68 (q, J = 6.8 Hz, 1H, CH), 2.43 (d, J = 6.8 Hz, 2H, CH2), 1.88-1.78 (m, 1H, CH), 1.48 (d, J = 7.2 Hz, 3H, CH3), 0.88 (d, J = 6.4 Hz, 6H, CH3); after it is converted to methyl ester, its ee value is 90percent through the chiral GC analysis.
With C54H68IrNP(1+)*C32H12BF24(1-); hydrogen; caesium carbonate; In methanol; at 45℃; under 4500.45 Torr; for 0.166667h;Glovebox; Sealed tube; The catalyst (S)-5a (0.9mg, 0.0005mmol) and 2-4-isobutyl-acrylic acid 6a (102mg, 0.5mmol) were weighed from glove box and transferred into the reaction inner tube containing a stir bar. The tube was sealed as a spare. Cesium carbonate (82mg, 0.25mmol) and methanol (2mL) were added into the tube after fetching out the tube. The inner tube was placed in the hydrogenation reaction still. The original atmosphere was displaced with hydrogen atmosphere by inflating-deflating operation (3-5 times). The hydrogen pressure was ultimately set at 0.6MPa. At the temperature of 45 , the reaction was proceeded with stirring until the pressure stopped decreasing. After stopping stirring to release hydrogen and concentrating the system with rotary steaming, the pH value of the system was adjusted with 3 N hydrochloric acid until pH 3). The organic phases merged together were washed by sodium chloride solution and dried by anhydrous sodium sulfate. The drying agent was removed by suction filtration. The target product (R) 7a was obtained after solvent was removed by rotary steaming. The conversion rate was analyzed by 1H NMR and the ee value was analyzed by chiral GC after the product was transformed into corresponding methyl ester. The experimental results determined are listed in Table 2:
With C54H72IrNP(1+)*C32H12BF24(1-); hydrogen; caesium carbonate; In methanol; at 45℃; under 4500.45 Torr; for 0.166667h;Glovebox; Example 6 Asymmetric Hydrogenation of (R)-Isoibuprofen The catalyst (0.0005 mmol) and 2-4-isobutyl-acrylic acid 6a (102 mg, 0.5 mmol) were weighed from glove box and transferred into the reaction inner tube containing a stir bar. The tube was sealed as a spare. Cesium carbonate (82 mg, 0.25 mmol) and methanol (2 mL) were added into the tube after fetching out the tube. The inner tube was placed in the hydrogenation reaction still. The original atmosphere was displaced with hydrogen atmosphere by inflating-deflating operation (3-5 times). The hydrogen pressure was ultimately set at 0.6 MPa. At the temperature of 45, the reaction was proceeded with stirring until the pressure stopped decreasing. After stopping stirring to release hydrogen and concentrating the system with rotary steaming, the pH value of the system was adjusted with 3 N hydrochloric acid until pH<3. The mixture was extracted by ether (10 mL 3). The organic phases merged together were washed by sodium chloride solution and dried by anhydrous sodium sulfate. The drying agent was removed by suction filtration. The target product 7a was obtained after solvent was removed by rotary steaming. Melting point: 53-55. [alpha]D30?52 (c 2.0, ethanol); 1H NMR (400 MHz, CDCl3): delta 9.98 (brs, 1H, COOH), 7.24 (d, J=7.6 Hz, 2H, Ar?H), 7.12 (d, J=7.6 Hz, 2H, Ar?H), 3.73 (q, J=7.2 Hz, 1H, CH), 2.47 (d, J=7.2 Hz, 2H, CH2), 1.86 (septet, J=6.8 Hz, 1H, CH), 1.52 (d, J=7.2 Hz, 3H, CH3), 0.92 (d, J=6.4 Hz, 6H, CH3)} [0067] The conversion rate was analyzed by 1H NMR and the ee value was analyzed by chiral GC after the product was transformed into corresponding methyl ester. The experimental results determined are listed in Table 1:
 

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