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Methyl piperidine-4-carboxylate hydrochloride

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Products Intro: Product Name:Methyl 4-piperidinecarboxylate
CAS:7462-86-4
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CAS:7462-86-4
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CAS:7462-86-4
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CAS:7462-86-4
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Products Intro: Product Name:Methyl 4-piperidinecarboxylate
CAS:7462-86-4
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Methyl piperidine-4-carboxylate hydrochloride manufacturers

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
Methyl piperidine-4-carboxylate hydrochloride Structure
Methyl piperidine-4-carboxylate hydrochloride Chemical Properties
Melting point 160°C
Boiling point 85-90 °C
density 1.06
refractive index 1.465
Fp 89 °C
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
AppearanceWhite to off-white Solid
CAS DataBase Reference7462-86-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
MSDS Information
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
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
Methyl piperidine-4-carboxylate hydrochloride Preparation Products And Raw materials
Raw materialsMethanol-->N-Boc-Piperidine-4-carboxylic acid methyl ester-->Isonipecotic acid-->Hydrochloric acid-->Dichloromethane-->Ethyl acetate
Preparation ProductsMethyl 1-(2,2-diMethylpropanoyl)piperidine-4-carboxylate
Tag:Methyl piperidine-4-carboxylate hydrochloride(7462-86-4) Related Product Information
Isonipecotic acid N-Boc-Piperidine-4-carboxylic acid methyl ester Methyl carbamate Methyl anthranilate Methyl formate Methyl benzoate Methylparaben Methyl 2-bromobenzoate Methyl isonipecotate Methyl acetate Ethyl piperidine-3-carboxylate hydrochloride METHYL PIPECOLINATE HYDROCHLORIDE METHYL PIPERIDINE-3-CARBOXYLATE HYDROCHLORIDE PIPERIDINE-4-CARBOXYLIC ACID ETHYL ESTER HYDROCHLORIDE 4-Piperidinemethanol Isonipecotamide 4-PIPERIDINECARBOXYLIC ACID T-BUTYL ESTER HCL Ethyl 4-piperidinecarboxylate