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ChemicalBook >  Product Catalog >  Organic Chemistry >  Carboxylic acids and derivatives >  N-BOC-AMINO-PIPERIDINYL-1,1-CARBOXYLIC ACID

N-BOC-AMINO-PIPERIDINYL-1,1-CARBOXYLIC ACID

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N-BOC-AMINO-PIPERIDINYL-1,1-CARBOXYLIC ACID Basic information

Product Name:
N-BOC-AMINO-PIPERIDINYL-1,1-CARBOXYLIC ACID
Synonyms:
  • N-BOC-AMINO-PIPERIDINYL-1,1-CARBOXYLIC ACID
  • N-(TERT-BUTOXYCARBONYL)-AMINO-PIPERIDINYL-1,1-CARBOXYLIC ACID
  • N-BOC-Amino-piperidinyl-1,1-carboxylic acid,95%
  • 4-(tert-butoxycarbonyl)piperidine-4-carboxylic acid
  • 4-(Boc-aMino)piperidine-4-carboxylic Acid
  • 2-{[(tert-butoxy)carbonyl]aMino}piperidine-1-carboxylic acid
  • 4-[[(tert-butoxyl)carbonyl]amino]-4-piperidinecarboxylic acid
  • 4-[(2-methylpropan-2-yl)oxycarbonylamino]piperidine-4-carboxylic acid
CAS:
252720-31-3
MF:
C11H20N2O4
MW:
244.29
Mol File:
252720-31-3.mol
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N-BOC-AMINO-PIPERIDINYL-1,1-CARBOXYLIC ACID Chemical Properties

Boiling point:
410℃
Density 
1.18
refractive index 
1.4620 (estimate)
Flash point:
202℃
storage temp. 
2-8°C(protect from light)
pka
3.36±0.20(Predicted)
Appearance
White to off-white Solid
InChI
InChI=1S/C11H20N2O4/c1-10(2,3)17-9(16)13-11(8(14)15)4-6-12-7-5-11/h12H,4-7H2,1-3H3,(H,13,16)(H,14,15)
InChIKey
RAENIWWUAIMXSI-UHFFFAOYSA-N
SMILES
N1CCC(NC(OC(C)(C)C)=O)(C(O)=O)CC1
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26

MSDS

  • Language:English Provider:ACROS
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N-BOC-AMINO-PIPERIDINYL-1,1-CARBOXYLIC ACID Usage And Synthesis

Chemical Properties

White to off-white crystalline powder

Uses

N-Boc-amino-piperidinyl-1,1-carboxylic acid is used in pharmaceutical synthesis.

Synthesis

The synthesis of N-BOC-amino-piperidinyl-1,1-carboxylic acid usually starts with piperidine-4-carboxylic acid. Sodium bicarbonate and di-tert-butyl dicarbonate (Boc₂O) are added to the reaction system, and the amino protection reaction is carried out in a solvent such as tetrahydrofuran (THF) or 1,4-dioxane. The reaction is stirred at room temperature for several hours until the reaction is completed. Subsequently, the crude product is obtained by steps such as ethyl acetate extraction, pH adjustment of the aqueous phase, drying of the organic phase and reduced pressure concentration, and then purified by column chromatography using a mixed solvent of ethyl acetate and n-hexane as an eluent to finally obtain a high-purity target compound.

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