ChemicalBook--->CAS DataBase List--->290328-55-1

290328-55-1

290328-55-1 Structure

290328-55-1 Structure
IdentificationBack Directory
[Name]

4-Methanesulfonyl-piperidine
[CAS]

290328-55-1
[Synonyms]

EOS-61037
4-Methanesulfonyl-piperidine
4-(Methylsulfonyl)piperid...
Piperidine, 4-(Methylsulfonyl)-
4-Methanesulfonylpiperidine hydrochloride
4-(methylsulfonyl)piperidine hydrochloride
[EINECS(EC#)]

1533716-785-6
[Molecular Formula]

C6H13NO2S
[MDL Number]

MFCD11043260
[MOL File]

290328-55-1.mol
[Molecular Weight]

163.24
Chemical PropertiesBack Directory
[Boiling point ]

336.9±31.0 °C(Predicted)
[density ]

1.18±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,2-8°C
[pka]

9.22±0.10(Predicted)
[Appearance]

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

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302+H312+H332-H315
[Precautionary statements ]

P280-P301+P312-P362+P364
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

4-Methanesulfonyl-piperidine(290328-55-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-Piperidinecarboxylic acid, 4-(Methylsulfonyl)-, 1,1-diMethylethyl ester

189205-49-0

4-Methanesulfonyl-piperidine

290328-55-1

General procedure for the synthesis of 4-methylsulfonylpiperidine from tert-butyl 4-(methylsulfonyl)piperidine-1-carboxylate (Step 4): tert-butyl 4-(methylsulfonyl)piperidine-1-carboxylate obtained in Step 3 of Reference Example 12 was dissolved in ethyl acetate (16 mL), followed by the addition of a 4.0 mol/L dioxane solution of hydrogen chloride (12 mL). The reaction mixture was stirred at room temperature for 3 hours. Upon completion of the reaction, the precipitated solid was collected by filtration to afford the target product 4-(methylsulfonyl)piperidine (1.4 g, 76% yield). The structure of the product was confirmed by 1H-NMR (DMSO-d6, 270 MHz) with the following chemical shifts δ (ppm): 3.41-3.31 (m, 3H), 2.97 (s, 3H), 2.97-2.82 (m, 2H), 2.18-2.13 (m, 2H), 1.92-1.73 (m, 2H).

[References]

[1] Patent: EP1642880, 2006, A1. Location in patent: Page/Page column 112
[2] Patent: US2003/100567, 2003, A1
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