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Chemical Structure| 101084-06-4 Chemical Structure| 101084-06-4

Structure of 101084-06-4

Chemical Structure| 101084-06-4

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Product Details of [ 101084-06-4 ]

CAS No. :101084-06-4
Formula : C7H6Cl3N
M.W : 210.49
SMILES Code : NCC1=C(Cl)C=C(Cl)C=C1Cl
MDL No. :MFCD00052914

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Application In Synthesis of [ 101084-06-4 ]

* 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 [ 101084-06-4 ]

[ 101084-06-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6575-05-9 ]
  • [ 101084-06-4 ]
YieldReaction ConditionsOperation in experiment
With borane-THF; In tetrahydrofuran; at 40℃; for 2h; A.2.26 Synthesis of (2,4,6-trichlorophenyl)methanamine To a solution of <strong>[6575-05-9]2,4,6-trichlorobenzonitrile</strong> (0.69 mmol) in 2 mL THF was added a solution of BH3 (2.77 mmol, 1 M in THF). The reaction mixture was heated to 40C for 2 h and then cooled to RT. 1 mL MeOH was added and the mixture was stirred at RT for 30 min. Water was added, the mixture was basified with 1 M NaOH solution and extracted twice with EtOAc. The combined organic layers were dried over MgS04 and concentrated in vacuo to give the desired product as slightly yellow oil. LC-MS (C): tR = 0.51 min; [M+H]+: 210.13.
To a solution of <strong>[6575-05-9]2,4,6-trichlorobenzonitrile</strong> (0.69 mmol) in 2 mL THF was added a solution of BH3 (2.77 mmol, 1M in THF). The reaction mixture was heated to 40 C. for 2 h and then cooled to RT. 1 mL MeOH was added and the mixture was stirred at RT for 30 min. Water was added, the mixture was basified with 1M NaOH solution and extracted twice with EtOAc. The combined organic layers were dried over MgSO4 and concentrated in vacuo to give the desired product as slightly yellow oil. LC-MS (C): tR=0.51 min; [M+H]+: 210.13.
 

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