3-METHYL-2-PYRROLIDINONE

3-METHYL-2-PYRROLIDINONE Suppliers list
Company Name: Capot Chemical Co., Ltd  
Tel: +86 (0) 571 85 58 67 18
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Company Name: Tetranov Biopharm  
Tel: 13526569071
Email: sales@leadmedpharm.com
Company Name: Shanghai Longsheng chemical Co.,Ltd.  
Tel: 58099637 13585536065
Email: sales@shlschem.com
Company Name: China DongFan Chemical Co.,LTD  
Tel: 86-0571-85151182
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Company Name: Shanghai Sunway Pharmaceutical Technology Co., Ltd  
Tel: 13761987713
Email: hxzheng@sunwaypharm.cn

3-METHYL-2-PYRROLIDINONE manufacturers

3-METHYL-2-PYRROLIDINONE Basic information
Product Name:3-METHYL-2-PYRROLIDINONE
Synonyms:(R,S)-3-Methyl-pyrrolidin-2-one;2-Pyrrolidinone,3-methyl-;α-Methylbutyrolactam;3-METHYL-2-PYRROLIDINONE;alpha-Methylbutyrolactam~3-Methyl-2-pyrrolidone;alpha-Methylbutyrolactame;3-Methyl-2-pyrrolidone;3-methylpyrrolidin-2-one
CAS:2555-05-7
MF:C5H9NO
MW:99.13
EINECS:219-865-2
Product Categories:Pyrrolidines
Mol File:2555-05-7.mol
3-METHYL-2-PYRROLIDINONE Structure
3-METHYL-2-PYRROLIDINONE Chemical Properties
Melting point 55°C
Boiling point 118-120 °C(Press: 10 Torr)
density 0.979±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka16.66±0.40(Predicted)
AppearanceWhite to off-white Solid
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
MSDS Information
ProviderLanguage
ALFA English
3-METHYL-2-PYRROLIDINONE Usage And Synthesis
Synthesis Reference(s)Tetrahedron, 43, p. 1811, 1987 DOI: 10.1016/S0040-4020(01)81492-7
Synthesis
1-Benzyl-3-methylpyrrolidin-2-one

108303-99-7

3-METHYL-2-PYRROLIDINONE

2555-05-7

1-Benzyl-3-methylpyrrolidin-2-one (0.323 g, 1.7 mmol, 1.0 eq.) was used as a starting material and dissolved in toluene (2 mL, 1 M). Trifluoromethanesulfonic acid (0.604 mL, 6.8 mmol, 4.0 eq.) was added to this solution. The reaction mixture was placed in a microwave reactor and heated at 195°C for 25 minutes. Upon completion of the reaction, the mixture was poured into a small amount of saturated aqueous sodium bicarbonate solution for neutralization. The aqueous phase was extracted with ethyl acetate and the organic phase was again washed with saturated aqueous sodium chloride solution. The combined aqueous phases were again extracted with ethyl acetate. All organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated in vacuum. The crude product was purified by silica gel column chromatography with a gradient of dichloromethane solution of 0-10% methanol as eluent to give 3-methyl-2-pyrrolidinone (0.087 g). The structure of the product was confirmed by 1H NMR (300 MHz, CDCl3): δ 6.49 (br s, 1H), 3.37-3.26 (m, 2H), 2.53-2.28 (m, 2H), 1.80-1.65 (m, 1H), 1.21-1.19 (d, 3H, J = 6.6 Hz).

References[1] Patent: US2015/284362, 2015, A1. Location in patent: Paragraph 0299
[2] Bioorganic and Medicinal Chemistry Letters, 2018, vol. 28, # 3, p. 293 - 297
Tag:3-METHYL-2-PYRROLIDINONE(2555-05-7) Related Product Information
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