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Chemical Structure| 168539-99-9 Chemical Structure| 168539-99-9

Structure of 168539-99-9

Chemical Structure| 168539-99-9

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Product Details of [ 168539-99-9 ]

CAS No. :168539-99-9
Formula : C11H19NO3
M.W : 213.27
SMILES Code : O=CC1(NC(OC(C)(C)C)=O)CCCC1
MDL No. :MFCD04973956

Safety of [ 168539-99-9 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H315-H318-H335-H400
Precautionary Statements:P261-P273-P280-P305+P351+P338
Class:9
UN#:3077
Packing Group:

Application In Synthesis of [ 168539-99-9 ]

* 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 [ 168539-99-9 ]

[ 168539-99-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 168539-99-9 ]
  • [ 94-98-4 ]
  • [ 439151-71-0 ]
YieldReaction ConditionsOperation in experiment
57% With sodium cyanoborohydride; In methanol; trimethyl orthoformate; (190a) To a solution of 1-[1,1-(dimethyl)ethoxycarbonyl]aminocyclopentyl carboxaldehyde (D. Braghiroli and M. Di Bella, Tetrahedron Lett. 1996, 37, 7319; 1.10 g, 5.16 mmol) in trimethyl orthoformate (20 mL) was added <strong>[94-98-4]2,4-dimethylbenzylamine</strong> (1.4 g) and the reaction mixture stirred at room temperature for 8 h. Sodium cyanoborohydride (0.96 g) and methanol (2.5 mL) were added consecutively and the suspension stirred at room temperature for 12 h. The mixture was quenched with water and extracted with dichloromethane (2*). The organic extracts were washed with brine, dried (Na2SO4), and concentrated in vacuo. Purification by flash chromatography (SiO2) provided N-Boc 1-[[(2,4-dimethylphenyl)methyl]amino]methylcyclopentylamine (974 mg, 57%) MS found: (M+H)+=333.
 

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