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1005-85-2

1005-85-2 Structure

1005-85-2 Structure
IdentificationMore
[Name]

3,3-PENTAMETHYLENE-2-PYRROLIDINONE
[CAS]

1005-85-2
[Synonyms]

1,1-Cyclohexane diacetimide
3,3-PENTAMETHYLENE-2-PYRROLIDINONE
3,3-PENTAMETHYLENE GLUTARIMIDE
3-AZASPIRO[5.5]UNDECANE-2,4-DIONE
CAI
[EINECS(EC#)]

214-459-1
[Molecular Formula]

C9H15NO
[MDL Number]

MFCD08063849
[Molecular Weight]

153.22
[MOL File]

1005-85-2.mol
Chemical PropertiesBack Directory
[Melting point ]

110 °C
[Boiling point ]

148-152 °C(Press: 1-2 Torr)
[density ]

1.05±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

16.27±0.20(Predicted)
[Appearance]

White to off-white Solid
[CAS DataBase Reference]

1005-85-2(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

3,3-PENTAMETHYLENE-2-PYRROLIDINONE(1005-85-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-cyanoMethyl-cyclohexanecarboxylic acid Methyl ester

956122-75-1

3,3-PENTAMETHYLENE-2-PYRROLIDINONE

1005-85-2

A reaction mixture was prepared from methyl 1-cyanomethyl-cyclohexanecarboxylate (4.28 g, 23.6 mmol) and cobalt(II) chloride hexahydrate (2.81 g, 11.8 mmol) in a solvent mixture of THF (80 mL) and water (40 mL) at 0 °C. Subsequently, sodium borohydride (4.47 g, 0.118 mol) was added in batches and the reaction mixture was slowly warmed to room temperature and stirred under nitrogen protection for 48 hours. Upon completion of the reaction, the reaction was quenched by the addition of 28% ammonium hydroxide solution (3.1 mL) and filtered through Hyflo. The filtrate was concentrated under reduced pressure and the residue was diluted with minimal amounts of water and brine and then extracted three times with 3:1 chloroisopropanol. The organic layers were combined, dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography using a gradient elution with a dichloromethane solution of 0 to 10% methanol to give 2-azaspiro[4.5]decan-1-one 1.95 g (54% yield). Thin layer chromatography (TLC) Rf value was 0.46 (unfolding agent: 9/1 dichloromethane/methanol). Mass spectrometry (MS) showed a molecular ion peak m/z: 154 (M+).

[References]

[1] Patent: WO2007/127763, 2007, A2. Location in patent: Page/Page column 33; 40
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