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Chemical Structure| 17797-12-5 Chemical Structure| 17797-12-5

Structure of 17797-12-5

Chemical Structure| 17797-12-5

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Product Details of [ 17797-12-5 ]

CAS No. :17797-12-5
Formula : C9H12BrN
M.W : 214.10
SMILES Code : CC(N)(C1=CC=C(Br)C=C1)C
MDL No. :MFCD06797600
InChI Key :IQKKTIWXHJDLFL-UHFFFAOYSA-N
Pubchem ID :23009116

Safety of [ 17797-12-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 17797-12-5 ]

* 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 [ 17797-12-5 ]

[ 17797-12-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24424-99-5 ]
  • [ 17797-12-5 ]
  • [ 214973-83-8 ]
YieldReaction ConditionsOperation in experiment
In tetrahydrofuran; at 20℃; for 16h; MeLi (2eq) is added to a solution of 4-bromo-benzonitrile (leq) an CeCi3 (leq) in THF at -78C. The reaction is allowed to warm to room temperature. Boc anhydride is added to the reaction. The solution is allowed to stir for 16 hrs at room temperature. Water, followed by EtOAc are added. The combined organic layers are separated, dried (MgSO/i) and concentrated in vacuo to give the desired product which is purified by column chromatography.
With triethylamine; In tetrahydrofuran; at 20℃; for 4h; Intermediate 201 [1-(4-Bromo-phenyl)-1-methyl-ethyl]-carbamic acid tert-butyl ester; To a solution of 1-(4-bromo-phenyl)-1-methyl-ethylamine (Intermediate 197) (1 eq, 10.8 mmol, 2.34 g) in THF (50 ml) are added TEA (1.5 eq, 16.2 mmol, 2.26 ml) and Boc2O (1.1 eq, 11.9 mmol, 2.6 g). The resulting mixture is stirred for 4 h at r.t. The solvents are evaporated, sat. aqueous NaCl solution is added, and the mixture is extracted with DCM. The combined organic layers are dried with MgSO4, filtered, and the solvents are removed under reduced pressure giving the title compound; [M+H]+=314/316.
 

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