4-Hydroxypiperidine hydrochloride
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
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)
MSDS
- Language:English Provider:SigmaAldrich
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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