Basic information Safety Supplier Related

PIPERIDINE-1-SULFONYL CHLORIDE

Basic information Safety Supplier Related

PIPERIDINE-1-SULFONYL CHLORIDE Basic information

Product Name:
PIPERIDINE-1-SULFONYL CHLORIDE
Synonyms:
  • piperidine-1-sulfonyl chloride(SALTDATA: FREE)
  • Piperadine-1-sulfonylchloride
  • N-piperidinylsulfaMoyl chloride
  • 1-Piperidinesulfonylchloride
  • Piperidinesulfonyl chloride
  • Piperidinosulfonyl chloride
  • Piperidine-1-Sulfonic Acid
  • Piperidine-1-sulfonyl chloride 96%
CAS:
35856-62-3
MF:
C5H10ClNO2S
MW:
183.66
Mol File:
35856-62-3.mol
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PIPERIDINE-1-SULFONYL CHLORIDE Chemical Properties

Boiling point:
120℃ (10 Torr)
Density 
1.308 g/mL at 25 °C
refractive index 
1.4920
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
-8.25±0.20(Predicted)
form 
liquid
color 
Dark brown
Sensitive 
Moisture Sensitive
InChIKey
QQJYAXDCMMXECR-UHFFFAOYSA-N
CAS DataBase Reference
35856-62-3
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-36/37/39-45
RIDADR 
UN 3265 8 / PGII
WGK Germany 
3
HazardClass 
8
HazardClass 
IRRITANT
PackingGroup 
HS Code 
2933399990
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PIPERIDINE-1-SULFONYL CHLORIDE Usage And Synthesis

Uses

Piperidine-1-sulfonyl chloride is used as pharmaceutical intermediate.

Synthesis

110-89-4

35856-62-3

Example 1: Synthesis of piperidine-1-sulfonyl chloride A mixture of piperidine (100 g, 1.17 mol) and triethylamine (178 g, 1.76 mol) in dichloromethane (500 ml) was slowly added to a solution of sulfuryl chloride (238 g, 1.76 mol) in dichloromethane (500 ml) at 0 °C - 5 °C. The reaction mixture was gradually warmed to room temperature and stirred continuously for 2 hours. After completion of the reaction, the mixture was quenched by pouring into ice water. The organic layer was separated and washed with distilled water (2 x 5 v/v). The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to give an oily residue (151.3 g, 70% yield). The resulting product was characterized by nuclear magnetic resonance hydrogen spectroscopy (H NMR): H NMR (300 MHz, CDCl3) δ = 1.58-1.62 (m, 2H), 1.69-1.83 (m, 4H), 3.31-3.42 (m, 4H).

References

[1] Patent: WO2015/83066, 2015, A1. Location in patent: Page/Page column 11-12
[2] Journal of Fluorine Chemistry, 1982, vol. 20, p. 425 - 438
[3] Patent: WO2005/87721, 2005, A2. Location in patent: Page/Page column 81-82
[4] Archiv der Pharmazie (Weinheim, Germany), 1958, vol. 291, p. 7,11
[5] Bulletin de la Societe Chimique de France, 1936, vol. <5> 3, p. 2143,2146, 2149, 2150

PIPERIDINE-1-SULFONYL CHLORIDESupplier

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