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89895-06-7

89895-06-7 Structure

89895-06-7 Structure
IdentificationBack Directory
[Name]

4-acetylpiperidinium chloride
[CAS]

89895-06-7
[Synonyms]

4-acetylpiperidinium chloride
1-(Piperidin-4-yl)ethanone, HCl
4-Acetylpiperidine hydrochloride
4-Acetylpiperidine hydrochloride,98%
1-(4-Piperidyl)ethanone Hydrochloride
1-(4-Piperidinyl)ethanone hydrochloride
1-(Piperidin-4-yl)ethanone hydrochloride
Ethanone, 1-(4-piperidinyl)-, hydrochloride
Ethanone,1-(4-piperidinyl)-, hydrochloride (1:1)
ETHANONE,1-(4-PIPERIDINYL)-,HYDROCHLORIE (1 : 1)
[EINECS(EC#)]

289-528-2
[Molecular Formula]

C7H14ClNO
[MDL Number]

MFCD00044810
[MOL File]

89895-06-7.mol
[Molecular Weight]

163.645
Chemical PropertiesBack Directory
[Melting point ]

151-158°C
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

White to Off-White
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H315-H319
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

1-(4-Piperidinyl)ethanone is used in the synthesis of oral antagonists for the treatment of rheumatoid arthritis. Also used in the synthesis of p38 mitogen activated protein kinase.
[Synthesis]

4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester

206989-61-9

4-acetylpiperidinium chloride

89895-06-7

General procedure for the synthesis of 1-(4-piperidinyl)ethanone hydrochloride from 1-N-BOC-4-acetylpiperidine: To an anhydrous dichloromethane (5 mL) solution of 1-N-BOC-4-acetylpiperidine (350 mg, 1.54 mmol) was slowly added a dioxane solution (2 mL) of 4 M HCl at 0 °C. The reaction mixture was stirred continuously at 0°C for 2 hours. Upon completion of the reaction, the mixture was concentrated by rotary evaporator to afford 1-(4-piperidinyl)ethanone hydrochloride (260 mg, 100% yield) as a white solid, which could be used directly in the subsequent reaction without further purification.

[References]

[1] Patent: WO2013/96744, 2013, A1. Location in patent: Page/Page column 192
[2] Patent: EP3255042, 2017, A2. Location in patent: Paragraph 0209; 0213
Spectrum DetailBack Directory
[Spectrum Detail]

4-acetylpiperidinium chloride(89895-06-7)1HNMR
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