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Chemical Structure| 61995-18-4 Chemical Structure| 61995-18-4

Structure of 61995-18-4

Chemical Structure| 61995-18-4

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Product Details of [ 61995-18-4 ]

CAS No. :61995-18-4
Formula : C7H11NO3
M.W : 157.17
SMILES Code : O=C(N1CC(CCC1)=O)OC
MDL No. :MFCD13179062

Safety of [ 61995-18-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 61995-18-4 ]

* 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 [ 61995-18-4 ]

[ 61995-18-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 50606-58-1 ]
  • [ 79-22-1 ]
  • [ 61995-18-4 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In chloroform; at 0 - 20℃; for 1h; EXAMPLE 3; Step 1: To 1-benzyl-3-piperidone HCl salt hydrate (1 eq, 0.111 mol, 25 g) completely dissolved in chloroform (100 mL) and triethylamine (1.1 eq, 0.122 mol, 17 mL) was added methyl chloroformate (1.1 eq, 0.122 mol, 9.4 mL) dropwise at 0 C. After the dropwise addition was complete, additional methyl chloroformate (0.7 eq, 0.078 mol, 6 mL) was added, the reaction mixture warmed to room temperature, and stirred 1 h. The volatiles were removed in vacuo and the resulting residue was taken up in 1N HCl (100 mL) and washed with hexanes (3×70 mL). The aqueous layer was then extracted with ethyl acetate (3×100 mL), the combined ethyl acetate layers washed with brine (1×50 mL), dried (Na2SO4), and concentrated in vacuo to give 23 as an orange oil (10 g), which was used without further purification. Note: If the aqueous layer retains some product, it can be completely extracted using 10% isopropyl alcohol in chloroform.
 

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