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Chemical Structure| 1033819-08-7 Chemical Structure| 1033819-08-7

Structure of 1033819-08-7

Chemical Structure| 1033819-08-7

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Product Details of [ 1033819-08-7 ]

CAS No. :1033819-08-7
Formula : C14H25NO3
M.W : 255.35
SMILES Code : O=C(N1CCC(CCC)(C=O)CC1)OC(C)(C)C
MDL No. :MFCD24470695

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Application In Synthesis of [ 1033819-08-7 ]

* 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 [ 1033819-08-7 ]

[ 1033819-08-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1033819-08-7 ]
  • [ 1023595-19-8 ]
YieldReaction ConditionsOperation in experiment
With ammonia; In methanol; at 110℃; under 60804.1 Torr;Autoclave; The 30 g of tert-butyl 4-formyl-4- propylpiperidinecarboxylate was dissolved in methanol of saturated ammonia, and 15 g of Raney Ni was added. The reaction mixture was heated to 110 C and allowed to 80 atmospheres in 2 L of high-pressure autoclave. The mixture was filtered to remove the catalyst and the filtrate was concentrated to give residue which was purified by column chromatography to afford tert-butyl 3 , 8-diazaspiro [5,5 ]undecane-3-carboxylate.
With ammonia; In methanol; at 110℃; under 60804.1 Torr;Autoclave; Step D: tert-butyl 3,8-diazaspiro[5,Slundecane-3-carboxylate: The 30 g of tert-butyl 4-formyl-4- propylpiperidinecarboxylate was dissolved in methanol of saturated ammonia, and 15 g of RaneyNi was added. The reaction mixture was heated to 110 C and allowed to 80 atmospheres in 2 L of high-pressure autoclave. The mixture was filtered to remove the catalyst and the filtrate was concentrated to give residue which was purified by column chromatography to afford tert-butyl 3, 8-diazaspiro [5,5 ]undecane-3 -carboxylate.
 

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