Basic information Safety Supplier Related

4-Hydroxypiperidine hydrochloride

Basic information Safety Supplier Related

4-Hydroxypiperidine hydrochloride Basic information

Product Name:
4-Hydroxypiperidine hydrochloride
Synonyms:
  • PIPERIDIN-4-OL HYDROCHLORIDE
  • TIMTEC-BB SBB004192
  • 4-HYDROXYPIPERIDINE HYDROCHLORIDE
  • 4-PIPERIDINOL HYDROCHLORIDE
  • 4-PIPIRIDINOL HYDROCHLORIDE
  • 4-Hydroxypiperidine HCl
  • 4-hydroxypiperidinium chloride
  • piperidin-4-ol hcl
CAS:
5382-17-2
MF:
C5H12ClNO
MW:
137.61
EINECS:
226-374-7
Product Categories:
  • Piperidine
Mol File:
5382-17-2.mol
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4-Hydroxypiperidine hydrochloride Chemical Properties

Melting point:
155-157 °C(lit.)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
methanol: soluble25mg/mL, clear, colorless
form 
powder to crystaline
color 
White to Orange to Green
Water Solubility 
very faint turbidity
BRN 
3908995
CAS DataBase Reference
5382-17-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
3
HS Code 
29333990

MSDS

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4-Hydroxypiperidine hydrochloride Usage And Synthesis

Chemical Properties

White powder

Uses

4-Hydroxypiperidine, HCl

Uses

4-Hydroxypiperidine hydrochloride is suitable for use in the Ugi-multi component reaction (MCR) to study the use of miniaturised-synthesis and Total Analysis System (mSYNTAS) in solution phase synthesis and on-line analysis of Ugi-MCRs. It may be used in the synthesis of acetic acid-piperidine-4-yl ester.

General Description

4-Hydroxypiperidine hydrochloride is a piperidine derivative. The synthesis of 4-hydroxypiperidine has been reported. 4-Hydroxypiperidine participates in the synthesis of 4-(4′-hydroxypiperidino)-4-phenylcyclohexanol and 1-(4-hydroxypiperidino)cyclohexanecarbonitrile. 4-Hydroxypiperidine is the starting material for the synthesis of Sibrafiban and Lamifiban, two non-peptidefibrinogen receptor.

Synthesis

109384-19-2

5382-17-2

The general procedure for the synthesis of 4-hydroxypiperidine hydrochloride from N-Boc-4-hydroxypiperidine was as follows: tert-butyl 4-hydroxypiperidine-1-carboxylate (5 g, 24.84 mmol, 1.00 eq.) was mixed with a saturated HCl solution dissolved in 30 mL of 1,4-dioxane, and the reaction was stirred for 2 h at room temperature. Upon completion of the reaction, the mixture was concentrated in vacuum to afford 4-hydroxypiperidine hydrochloride (3.4 g, 99% yield) as an off-white solid.

References

[1] Patent: WO2015/52264, 2015, A1. Location in patent: Paragraph 0918; 0919
[2] Patent: WO2017/153520, 2017, A1. Location in patent: Page/Page column 50
[3] Patent: WO2016/34673, 2016, A1. Location in patent: Page/Page column 120

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