ChemicalBook--->CAS DataBase List--->4842-86-8

4842-86-8

4842-86-8 Structure

4842-86-8 Structure
IdentificationBack Directory
[Name]

Ethyl piperidine-3-carboxylate hydrochloride
[CAS]

4842-86-8
[Synonyms]

ETHYL NIPECOTATE HYDROCHLORIDE
Ethyl 3-Piperidine-Carboxylate HCl
Ethyl piperidine-3-carboxylate HCl
ETHYL 3-PIPERIDINECARBOXYLATE HYDROCHLORIDE
3-Piperidine Carboxylic Acid Ethyl Ester HCl
Ethyl piperidine-3-carboxylate hydrochloride
Ethyl 3-piperidinecarboxylicester hydrochloride
RS-3-Piperidinecarboxylic acid ethyl ester hydrochloride
[EINECS(EC#)]

203-126-8
[Molecular Formula]

C8H16ClNO2
[MDL Number]

MFCD09032960
[MOL File]

4842-86-8.mol
[Molecular Weight]

193.67
Chemical PropertiesBack Directory
[Melting point ]

100-102°C
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl piperidine-3-carboxylate hydrochloride(4842-86-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethanol

64-17-5

Nipecotic acid

498-95-3

Ethyl piperidine-3-carboxylate hydrochloride

4842-86-8

Example 171A Synthesis of 3-(ethoxycarbonyl)piperidine hydrochloride: thionyl chloride (22.5 mL) was slowly added dropwise to a solution of ethanol (40 mL) containing piperidine-3-carboxylic acid (10.7 g, 83 mmol) at 0 °C. Subsequently, the reaction mixture was heated to reflux and kept reacting overnight. Upon completion of the reaction, the solvent was removed by evaporation under reduced pressure to afford the target product 3-(ethoxycarbonyl)piperidine hydrochloride (13 g, yield: 100%). The product was analyzed by LC-MS (ESI) and showed m/z: 158 ([M+H]+).

[References]

[1] Patent: US2009/197863, 2009, A1. Location in patent: Page/Page column 80
[2] Patent: WO2018/26779, 2018, A1. Location in patent: Page/Page column 30; 31
[3] Patent: US2009/62268, 2009, A1. Location in patent: Page/Page column 47-48
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