ChemicalBook--->CAS DataBase List--->577780-05-3

577780-05-3

577780-05-3 Structure

577780-05-3 Structure
IdentificationBack Directory
[Name]

2-Pyrrolidinone,3-(hydroxymethyl)-1-methyl-(9CI)
[CAS]

577780-05-3
[Synonyms]

3-(hydroxyMethyl)-1-Methyl-2-Pyrrolidinone
3-(HydroxyMethyl)-1-Methylpyrrolidin-2-one
2-Pyrrolidinone, 3-(hydroxymethyl)-1-methyl-
2-Pyrrolidinone,3-(hydroxymethyl)-1-methyl-(9CI)
[Molecular Formula]

C6H11NO2
[MDL Number]

MFCD18816870
[MOL File]

577780-05-3.mol
[Molecular Weight]

129.16
Chemical PropertiesBack Directory
[Boiling point ]

281.8±13.0 °C(Predicted)
[density ]

1.124±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

14.33±0.10(Predicted)
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

2-Pyrrolidinone,3-(hydroxymethyl)-1-methyl-(9CI)(577780-05-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Pyrrolidinone, 1-methyl-3-[(phenylmethoxy)methyl]-

577780-04-2

2-Pyrrolidinone,3-(hydroxymethyl)-1-methyl-(9CI)

577780-05-3

3-[(Benzyloxy)methyl]-1-methylpyrrolidin-2-one (4.14 g, 18.88 mmol) was used as a raw material and dissolved in methanol (20 mL). Subsequently, 10% aqueous palladium carbon (1.04 g) was added and the reaction mixture was stirred at 0 °C. The reaction mixture was stirred at room temperature for 2 hours under hydrogen atmosphere. Upon completion of the reaction, the palladium carbon catalyst was removed by filtration and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography with the eluent ethyl acetate/methanol (10:1, v/v) to afford 1-methyl-3-(hydroxymethyl)-2-pyrrolidinone (1.55 g, 64% yield) as a colorless oil.1H-NMR (CDCl3) δ: 1.7-1.9 (1H, m), 2.05-2.25 (1H, m), 2.6 -2.8 (1H, m), 2.86 (3H, s), 3.25-3.45 (3H, m), 3.65-3.95 (2H, m).

[References]

[1] Patent: EP1479684, 2004, A1. Location in patent: Page 20
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