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Chemical Structure| 21962-46-9 Chemical Structure| 21962-46-9

Structure of 21962-46-9

Chemical Structure| 21962-46-9

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Product Details of [ 21962-46-9 ]

CAS No. :21962-46-9
Formula : C9H7NO2
M.W : 161.16
SMILES Code : N#CC1=CC(OC)=CC(C=O)=C1
MDL No. :MFCD18394186

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Application In Synthesis of [ 21962-46-9 ]

* 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 [ 21962-46-9 ]

[ 21962-46-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 557-21-1 ]
  • [ 262450-65-7 ]
  • [ 21962-46-9 ]
YieldReaction ConditionsOperation in experiment
tetrakis(triphenylphosphine) palladium(0); In N,N-dimethyl-formamide; at 90℃; for 48h; step 3-A solution of <strong>[262450-65-7]3-bromo-5-methoxy-benzaldehyde</strong> (1 mmol) in DMF (2 mL) is added to a round bottomed flask containing Zn(CN)2 (0.7 equivalents), Pd(PPh3)4(0) (0.2 equivalents) in DMF (15 mL). The reaction is stirred at 90 C. under an atmosphere of argon for 48 h. The reaction mixture is cooled and evaporated to dryness. The crude residue is dissolved in EtOAc, washed with brine solution, dried (MgSO4) and evaporated. The crude product is purified by SiO2 chromatography to afford 3-formyl-5-methoxy-benzonitrile.
tetrakis(triphenylphosphine) palladium(0); In N,N-dimethyl-formamide; at 90℃; for 48h; A solution of <strong>[262450-65-7]3-bromo-5-methoxy-benzaldehyde</strong> (1 mmol) in DMF (2 mL) is added to a round bottomed flask containing Zn(CN)2 (0.7 equivalents), Pd(PPh3)4(0) (0.2 equivalents) in DMF (15 mL). The reaction is stirred at 90 C. under an atmosphere of argon for 48 h. The reaction mixture is cooled and evaporated to dryness. The crude residue is dissolved in EtOAc, washed with brine solution, dried (MgSO4) and evaporated. The crude product is purified by SiO2 chromatography to afford 3-formyl-5-methoxy-benzonitrile.
tetrakis(triphenylphosphine) palladium(0); In N,N-dimethyl-formamide; at 90℃; for 48h; step 10-; Cyanation of 11 to afford 12a was carried out with Zn(CN)2, Pd(PPh3)4(O) and DMF. A solution of 11 (1 mmol) in DMF (2 mL) is added to a round bottomed flask containing Zn(CN)2 (0.7 equivalents), Pd(PPh3)4(O) (0.2 equivalents) in DMF (15 mL). The reaction is stirred at 90 C. under an atmosphere of argon for 48 h. The reaction mixture is cooled and evaporated to dryness. The crude residue is dissolved in EtOAc, washed with brine solution, dried (MgSO4) and evaporated. The crude product is purified by SiO2 chromatography
  • 2
  • [ 73963-98-1 ]
  • [ 262450-65-7 ]
  • [ 21962-46-9 ]
YieldReaction ConditionsOperation in experiment
tetrakis(triphenylphosphine) palladium(0); In N,N-dimethyl-formamide; at 80℃; for 5.5h; A solution of 21 (10 g, 31.7 mmol), Pd[P(Ph)3]4(0) (2.62 g, 2.26 mmol), Zn(CN)2(2.24 g, 19.0 mmol) and DMF (100 mL) under a N2 atmosphere is heated to 80 C. for 5.5 h. The reaction mixture is cooled to RT and is partitioned between water and DCM. The DCM extracts are washed with water and brine and is dried (MgSO4). The crude product is purified by SiO2 chromatography eluting with EtOAc/hexane to afford 22a.
 

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