1-AMINO-PIPERIDIN-4-OL

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CAS:79414-82-7
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CAS:79414-82-7
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1-AMINO-PIPERIDIN-4-OL Basic information
Product Name:1-AMINO-PIPERIDIN-4-OL
Synonyms:1-AMINO-PIPERIDIN-4-OL;1-aMino-4-Piperidinol;4-Piperidinol, 1-amino-
CAS:79414-82-7
MF:C5H12N2O
MW:116.16
EINECS:
Product Categories:
Mol File:79414-82-7.mol
1-AMINO-PIPERIDIN-4-OL Structure
1-AMINO-PIPERIDIN-4-OL Chemical Properties
Boiling point 86 °C(Press: 0.15 Torr)
density 1.137±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka15.11±0.20(Predicted)
AppearanceLight yellow to yellow Solid
Safety Information
MSDS Information
1-AMINO-PIPERIDIN-4-OL Usage And Synthesis
Synthesis
N-nitroso-4-hydroxypiperidine

55556-93-9

1-AMINO-PIPERIDIN-4-OL

79414-82-7

General procedure for the synthesis of 1-amino-4-piperidinol from 1-nitrosopiperidin-4-ol: 14 g of 1-amino-4-piperidinol was prepared; lithium aluminum hydride (LAH, 1.0 M, 175 mL) was added batchwise to a tetrahydrofuran (THF, 250 mL) solution of 1-nitrosopiperidin-4-ol (12.9 g) over 40 min. After the addition was completed, the reaction mixture was refluxed for 3 h and subsequently cooled to room temperature and further cooled to 0 °C in an ice bath. The reaction mixture was gradually warmed to room temperature by slowly adding water (40 mL), held for 10 min, and then refluxed for 30 min. The precipitate was collected by filtration, suspended in hot THF (100 mL) and filtered again. All the filtrates were combined, dried with anhydrous sodium sulfate, filtered and concentrated to give the target product 1-amino-4-piperidinol in the form of a light yellow oil. Yield: 10.7 g, 94% yield.

References[1] Patent: WO2007/127688, 2007, A2. Location in patent: Page/Page column 38; 47-48
[2] Patent: US2006/4055, 2006, A1. Location in patent: Page/Page column 1-2
1-AMINO-PIPERIDIN-4-OL Preparation Products And Raw materials
Raw materialsN-nitroso-4-hydroxypiperidine-->4-Hydroxypiperidine-->Lithium Aluminum Hydride-->Tetrahydrofuran-->Water
Tag:1-AMINO-PIPERIDIN-4-OL(79414-82-7) Related Product Information
4'-HYDROXY-[1,1']BIPIPERIDINYL-3-CARBOXYLIC ACID AMIDE 1-Piperidinamine,4-methoxy-(9CI) N-nitroso-4-hydroxypiperidine 1-AMINO-PIPERIDIN-4-OL

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