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Chemical Structure| 125867-26-7 Chemical Structure| 125867-26-7

Structure of 125867-26-7

Chemical Structure| 125867-26-7

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Product Details of [ 125867-26-7 ]

CAS No. :125867-26-7
Formula : C17H20N2O2
M.W : 284.35
SMILES Code : CC(C)(C)C(NC1=C(C(O)C2=CC=CC=C2)C=NC=C1)=O
MDL No. :MFCD18213844

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Application In Synthesis of [ 125867-26-7 ]

* 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 [ 125867-26-7 ]

[ 125867-26-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 70298-89-4 ]
  • [ 100-52-7 ]
  • [ 125867-26-7 ]
YieldReaction ConditionsOperation in experiment
To a solution of 2.33 g (13.1 mmol, 1 eq.) of pivalamide VII and 5.9 mL (39.2 mmol, 3 eq.) of TMEDA in 105 mL of diethylether, cooled to -78°C, were added 15.7 mL (39.2 mmol, 3 eq., 2.5 M in hexane) of BuLi. After 15 minutes, the solution was brought back to -24°C and stirred 2 hours. Then, the mixture was cooled down to - 78°C before addition of 2.9 mL (28.8 mmol, 2.2 eq) of benzaldehyde in 50 mL of THF. The reaction was brought back to 0°C and stirred 2 hours before being stirred at room temperature over night. Then, 100 mL of water were added. The aqueous layer was extracted with 3 x 60 mL of dichloromethane. The organic phase was dried, filtered and concentrated. The crude mixture was purified over silica gel (PE/EtOAc 2:1 ) and the mixture (2 products, including VIII) was dissolved in 50 mL of DCM. Then, 2.30 g (26.4 mmol) of activated Mn02 were added and the reaction was refluxed 40 hours. The mixture was filtered on celite and the solvent was evaporated. The crude mixture was purified over silica gel (PE/EtOAc 1 :1 ). Then, 100 mL of 3 M aqueous HCI were added and refluxed 16 hours. The reaction was cooled down to 0°C and 50 mL of aqueous ammonia were added. The aqueous layer was extracted with 3 x 50 mL of DCM. The organic phase was dried, filtered and concentrated to yield 730 mg (3.7 mmol, 28percent) of IX as a white solid. Rf=0.12 (PE/EtOAc 1 :2). 1H NMR (300 MHz): delta = 8.58 (s, 1 H), 8.22 (d, J = 5.9 Hz, 1 H), 7.67 (m, 2 H), 7.57 (m, 1 H), 7.49 (m, 2 H), 6.60 (d, J = 5.9 Hz, 1 H), 6.56 (broad, 2 H) ppm. 13C NMR (75 MHz): delta = 198.5, 156.0, 155.6, 152.0, 139.0, 131.9, 129.3, 128.5, 115.0, 111.3 ppm
To a solution of 2.33 g (13.1 mmol, 1 eq.) of pivalamide VII and 5.9 mL (39.2 mmol, 3 eq.) of TMEDA in 105 mL of diethylether, cooled to -78°C, were added 15.7 mL (39.2 mmol, 3 eq., 2.5 M in hexane) of BuLi. After 15 minutes, the solution was brought back to -24°C and stirred 2 hours. Then, the mixture was cooled down to - 78°C before addition of 2.9 mL (28.8 mmol, 2.2 eq) of benzaldehyde in 50 mL of THF. The reaction was brought back to 0°C and stirred 2 hours before being stirred at room temperature over night. Then, 100 mL of water were added. The aqueous layer was extracted with 3 x 60 mL of dichloromethane. The organic phase was dried, filtered and concentrated. The crude mixture was purified over silica gel (PE/EtOAc 2:1 ) and the mixture (2 products, including VIII) was dissolved in 50 mL of DCM. Then, 2.30 g (26.4 mmol) of activated Mn02 were added and the reaction was refluxed 40 hours. The mixture was filtered on celite and the solvent was evaporated. The crude mixture was purified over silica gel (PE/EtOAc 1 :1 ). Then, 100 mL of 3 M aqueous HCI were added and refluxed 16 hours. The reaction was cooled down to 0°C and 50 mL of aqueous ammonia were added. The aqueous layer was extracted with 3 x 50 mL of DCM. The organic phase was dried, filtered and concentrated to yield 730 mg (3.7 mmol, 28percent) of IX as a white solid. Rf=0.12 (PE/EtOAc 1 :2). 1H NMR (300 MHz): delta = 8.58 (s, 1 H), 8.22 (d, J = 5.9 Hz, 1 H), 7.67 (m, 2 H), 7.57 (m, 1 H), 7.49 (m, 2 H), 6.60 (d, J = 5.9 Hz, 1 H), 6.56 (broad, 2 H) ppm. 13C NMR (75 MHz): delta = 198.5, 156.0, 155.6, 152.0, 139.0, 131.9, 129.3, 128.5, 115.0, 111.3 ppm
 

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