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Chemical Structure| 301673-14-3 Chemical Structure| 301673-14-3
Chemical Structure| 301673-14-3

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Product Details of tert-Butyl 4-iodopiperidine-1-carboxylate

CAS No. :301673-14-3
Formula : C10H18INO2
M.W : 311.16
SMILES Code : O=C(N1CCC(I)CC1)OC(C)(C)C
MDL No. :MFCD04115041
InChI Key :YFWQFKUQVJNPKP-UHFFFAOYSA-N
Pubchem ID :10892302

Safety of tert-Butyl 4-iodopiperidine-1-carboxylate

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of tert-Butyl 4-iodopiperidine-1-carboxylate

* 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 [ 301673-14-3 ]

[ 301673-14-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 98-88-4 ]
  • [ 301673-14-3 ]
  • [ 193217-39-9 ]
  • 2
  • [ 176022-47-2 ]
  • [ 301673-14-3 ]
  • (S)-N-tert-butoxycarbonyl-4-[(4-chlorophenyl)(2-pyridyl)methoxy]piperidine [ No CAS ]
YieldReaction ConditionsOperation in experiment
84% N-tert-butoxycarbonyl-4-bromopiperidine in Example 1 was replaced by an equimolar amount of N-t-butoxycarbonyl-4-iodopiperidine,The same operation as in Example 1 was followed except that the yield of the product was 84%. (S) - (4-chlorophenyl) (2-pyridyl) -methanol 21.9 g (0.1 mol) of the formula (II)Was dissolved in 160 mL of tetrahydrofuran,41 g (0.1 mol) of sodium hydride in a mass fraction of 60% was added portionwise with stirring,Stirring for 2 hours to no bubbles,The reaction was allowed to cool under ice-coolingA solution of 26.4 g (0.1 mol) of N-t-butoxycarbonyl-4-bromopiperidine was added dropwise,After completion of the dropwise addition, the reaction was gradually warmed to room temperature with stirring for 5 hours,The reaction solution was added to 200 mL of saturated ammonium chloride solution,Stirred for 30 minutes,The reaction solution was extracted twice with 300 mL of ethyl acetate,The organic phases were combined,Dried over anhydrous sodium sulfate for 2 hours,filter,The mother liquor was evaporated to dryness to give 34.3 g of product,The product was directly subjected to the next reaction without purification,Yield 85%.
  • 3
  • [ 65-85-0 ]
  • [ 301673-14-3 ]
  • [ 193217-39-9 ]
 

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