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10441-57-3

10441-57-3 Structure

10441-57-3 Structure
IdentificationBack Directory
[Name]

1-METHYLPYRROLIDINE-2-THIONE
[CAS]

10441-57-3
[Synonyms]

1-METHYLPYRROLIDINE-2-THIONE
1-methyl-2-pyrrolidinethione
2-Pyrrolidinethione, 1-Methyl-
1-Methylpyrrolidine-2-thione>
1-METHYLPYRROLIDINE-2-THIONE 97.0%+(GC)
[Molecular Formula]

C5H9NS
[MDL Number]

MFCD00966332
[MOL File]

10441-57-3.mol
[Molecular Weight]

115.197
Chemical PropertiesBack Directory
[Melting point ]

16 °C
[Boiling point ]

145 °C / 15mmHg
[density ]

1.09
[refractive index ]

1.5830 to 1.5870
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

clear liquid
[pka]

1.74±0.20(Predicted)
[color ]

Light yellow to Brown
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H315
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

1-METHYLPYRROLIDINE-2-THIONE(10441-57-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

N-Methyl-2-pyrrolidone

872-50-4

1-METHYLPYRROLIDINE-2-THIONE

10441-57-3

The general procedure for the synthesis of 1-methylpyrrolidin-2-thione from N-methylpyrrolidone was as follows: N-methylpyrrolidone (0.75 mmol) was dissolved in tetrahydrofuran (THF, 5 mL) in a microwave reaction flask, followed by the addition of phosphorus pentasulfide/aluminum oxide (P2S5/Al2O3, 0.53 g, equivalent to 0.90 mmol of P2S5). After sealing the reaction vial, the suspension was placed in a CEM Discover? microwave reactor and heated by microwave radiation at 60 °C and 60 W power with stirring and air cooling. After 5 min of reaction, the completion of the reaction was confirmed by thin layer chromatography (TLC) monitoring. The reaction solution was cooled and quickly filtered through a short silica gel column. The reaction was first eluted with hexane to remove non-polar impurities, followed by a solvent mixture of hexane/ethyl acetate (EtOAc) to recover the target product 1-methylpyrrolidine-2-thione. Finally, the solvent was removed by distillation under reduced pressure to afford pure 1-methylpyrrolidine-2-thione in 92% yield.

[References]

[1] Organic Letters, 2012, vol. 14, # 2, p. 440 - 443
[2] Organic Syntheses, 1984, vol. 62, p. 158 - 158
[3] European Journal of Medicinal Chemistry, 1991, vol. 26, # 7, p. 687 - 697
[4] Tetrahedron, 1984, vol. 40, # 11, p. 2047 - 2052
[5] Tetrahedron Letters, 2011, vol. 52, # 40, p. 5131 - 5132
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