ChemicalBook--->CAS DataBase List--->79414-82-7

79414-82-7

79414-82-7 Structure

79414-82-7 Structure
IdentificationBack Directory
[Name]

1-AMINO-PIPERIDIN-4-OL
[CAS]

79414-82-7
[Synonyms]

1-aMino-4-Piperidinol
1-AMINO-PIPERIDIN-4-OL
[Molecular Formula]

C5H12N2O
[MDL Number]

MFCD07787036
[MOL File]

79414-82-7.mol
[Molecular Weight]

116.16
Chemical PropertiesBack Directory
[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
[pka]

15.11±0.20(Predicted)
[Appearance]

Light yellow to yellow Solid
Spectrum DetailBack Directory
[Spectrum Detail]

1-AMINO-PIPERIDIN-4-OL(79414-82-7)1HNMR
Hazard InformationBack Directory
[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
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