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N-BOC-3-Aminopiperidine

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N-BOC-3-Aminopiperidine Basic information

Product Name:
N-BOC-3-Aminopiperidine
Synonyms:
  • 3-AMINO-1-BOC-PIPERIDINE X HCL
  • N-Boc-3-piperidinamine
  • 1-Boc-3-aminopiperidinecitricacid
  • 1-BOC-3-aminopiperdine
  • 1-Boc-3-aminopiperidine ,97%
  • N-BOC-3-AMinopiperidine(HCl)
  • N-BOC-3-AMinopiperid
  • 3-Amino-1-Boc-piperidine tert-Butyl 3-Amino-1-piperidinecarboxylate 3-Amino-1-piperidinecarboxylic Acid tert-Butyl Ester
CAS:
184637-48-7
MF:
C10H20N2O2
MW:
200.28
Product Categories:
  • Piperidines
  • Chiral Reagent
  • Piperidine
  • pharmacetical
  • AMINOACID
  • Pharmaceutical Intermediates
Mol File:
184637-48-7.mol
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N-BOC-3-Aminopiperidine Chemical Properties

Melting point:
181-182°C
Boiling point:
277.3±33.0 °C(Predicted)
Density 
1.02
refractive index 
1.4710-1.4750
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
clear liquid
pka
10.35±0.20(Predicted)
color 
Colorless to Light yellow
optical activity
Consistent with structure
Water Solubility 
Slightly soluble in water.
Sensitive 
Air Sensitive
InChI
InChI=1S/C10H20N2O2/c1-10(2,3)14-9(13)12-6-4-5-8(11)7-12/h8H,4-7,11H2,1-3H3
InChIKey
AKQXKEBCONUWCL-UHFFFAOYSA-N
SMILES
N1(C(OC(C)(C)C)=O)CCCC(N)C1
CAS DataBase Reference
184637-48-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22-36/37/38-51
Safety Statements 
26-39-37
HazardClass 
IRRITANT
HS Code 
29335990
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N-BOC-3-Aminopiperidine Usage And Synthesis

Uses

3-Amino-1-Boc-piperidine is used as an organic chemical synthesis intermediate.

Synthesis

54012-73-6

24424-99-5

144243-24-3

184637-48-7

In a 200 mL four-necked flask equipped with a stirrer, pH sensor, and two dropping funnels, 90 g of ethanol and 10.0 g (0.1 mol) of 3-aminopiperidine were added and stirred at 10 to 15 °C. 21.8 g (0.1 mol) di-tert-butyl dicarbonate was slowly added through one dropping funnel while 17.6 g (0.11 mol) 25% aqueous sodium hydroxide was added dropwise through the other dropping funnel, and the dropping rate was controlled to maintain the pH of the reaction system between 11.8 and 12.2. The titration process was completed in about 1 hour. Upon completion of the reaction, the composition of the reaction mixture was analyzed and confirmed to contain 6% unreacted 3-aminopiperidine, 91.5% of the target product 3-amino-1-tert-butoxycarbonylpiperidine and 1.1% of the by-product 3-tert-butoxycarbonylaminopiperidine.

References

[1] Patent: EP1460061, 2004, A1. Location in patent: Page 6-7

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