ChemicalBook--->CAS DataBase List--->7462-86-4

7462-86-4

7462-86-4 Structure

7462-86-4 Structure
IdentificationMore
[Name]

Methyl 4-piperidinecarboxylate
[CAS]

7462-86-4
[Synonyms]

METHYL 4-PIPERIDINECARBOXYLATE HCL
METHYL ISONIPECOTATE HYDROCHLORIDE
METHYL ISONIPECOTINATE HYDROCHLORIDE
Methyl Isonipecotate HCl
Methyl 4-Piperidinecarboxylic Ester HCl
Methyl 4-piperidinecarboxylate hydrochloride
methyl piperidine-4-carboxylate hydrochloride
4-PIPERIDINECARBOXYLIC ACID METHYL ESTER HYDROCHLORIDE
Methyl 4-piperidinecarboxylicester hydrochloride
METHYL PIPERIDINE-4-CARBOXYLATE HCL
[EINECS(EC#)]

203-126-8
[Molecular Formula]

C7H13NO2
[MDL Number]

MFCD02667641
[Molecular Weight]

143.18
[MOL File]

7462-86-4.mol
Chemical PropertiesBack Directory
[Melting point ]

160°C
[Boiling point ]

85-90 °C
[density ]

1.06
[refractive index ]

1.465
[Fp ]

89 °C
[storage temp. ]

Inert atmosphere,2-8°C
[Appearance]

White to off-white Solid
[CAS DataBase Reference]

7462-86-4(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319
[Precautionary statements ]

P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
Hazard InformationBack Directory
[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]

N-Boc-Piperidine-4-carboxylic acid methyl ester

124443-68-1

Methyl piperidine-4-carboxylate hydrochloride

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
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl piperidine-4-carboxylate hydrochloride(7462-86-4)1HNMR
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