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Methyl piperidine-4-carboxylate hydrochloride

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Methyl piperidine-4-carboxylate hydrochloride Basic information

Product Name:
Methyl piperidine-4-carboxylate hydrochloride
Synonyms:
  • METHYL ISONIPECOTATE HYDROCHLORIDE
  • METHYL ISONIPECOTINATE HYDROCHLORIDE
  • METHYL 4-PIPERIDINECARBOXYLATE HCL
  • Methyl Isonipecotate HCl
  • Methyl 4-Piperidinecarboxylic Ester HCl
  • Methyl 4-piperidinecarboxylate hydrochloride
  • methyl piperidine-4-carboxylate hydrochloride
  • 4-PIPERIDINECARBOXYLIC ACID METHYL ESTER HYDROCHLORIDE
CAS:
7462-86-4
MF:
C7H14ClNO2
MW:
179.64
EINECS:
203-126-8
Product Categories:
  • Pyrans, Piperidines & Piperazines
  • Esters
  • Pyrans, Piperidines &Piperazines
Mol File:
7462-86-4.mol
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Methyl piperidine-4-carboxylate hydrochloride Chemical Properties

Melting point:
160°C
Boiling point:
85-90 °C
Density 
1.06
refractive index 
1.465
Flash point:
89 °C
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
White to off-white Solid
CAS DataBase Reference
7462-86-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
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Methyl piperidine-4-carboxylate hydrochloride Usage And Synthesis

Uses

Methyl piperidine-4-carboxylate hydrochloride is a crucial compound that could be used as a pharmaceutical intermediate in pharmaceutical synthesis and scientific research.

Synthesis

124443-68-1

7462-86-4

General procedure for the synthesis of methyl 4-piperidinecarboxylate hydrochloride from methyl 1-tert-butoxycarbonyl-4-piperidinecarboxylate: To a dichloromethane (DCM, 3 mL) solution of methyl 1-tert-butoxycarbonyl-4-piperidinecarboxylate (2.16 g, 8.88 mmol) was added a solution of ethyl acetate (EtOAc, 6 mL) of 4 M hydrochloric acid. The reaction mixture was stirred at room temperature for 1.5 h. Subsequent removal of the solvent by concentration under reduced pressure afforded methyl 4-piperidinecarboxylate hydrochloride as a white solid (1.59 g, 99% yield). The product was characterized by 1H NMR (400 MHz, CD3OD): δ 3.73 (s, 3H), 3.44-3.39 (m, 2H), 3.15-3.09 (m, 2H), 2.82-2.77 (m, 1H), 2.21-2.16 (m, 2H), 1.99-1.89 (m, 2H); MS-ESI: m/z 144.2 [M + H - HCl]+.

References

[1] Patent: WO2016/34134, 2016, A1. Location in patent: Paragraph 00373
[2] Patent: CN105399698, 2016, A. Location in patent: Paragraph 0920-0923

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