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1585-90-6

1585-90-6 Structure

1585-90-6 Structure
IdentificationBack Directory
[Name]

1-(2-HYDROXY-ETHYL)-PYRROLE-2,5-DIONE
[CAS]

1585-90-6
[Synonyms]

HEMI
N-(Ethanol)maleimide
N-Hydroxyethyl MaleiMide
N-hydroxyethylMaleiciMide
1-(2-Hydroxyethyl)maleimide
N-(2-HYDROXYETHYL)MALEIMIDE
N-(2-Hydroxyethyl)MaleiMide 97%
N-(2-Hydroxyethyl)MaleiMide,99%
1-(2-HYDROXY-ETHYL)-PYRROLE-2,5-DIONE
1-(2-hydroxyethyl)-1H-pyrrole-2,5-dione
1H-Pyrrole-2,5-dione,1-(2-hydroxyethyl)-
N-(2-Hydroxyethyl)MaleiMide
[Molecular Formula]

C6H7NO3
[MDL Number]

MFCD00465266
[MOL File]

1585-90-6.mol
[Molecular Weight]

141.12
Chemical PropertiesBack Directory
[Melting point ]

70-71℃
[Boiling point ]

130°C/0.005mmHg(lit.)
[density ]

1.395
[storage temp. ]

2-8°C
[form ]

Powder
[pka]

14.21±0.10(Predicted)
[color ]

white
[InChI]

InChI=1S/C6H7NO3/c8-4-3-7-5(9)1-2-6(7)10/h1-2,8H,3-4H2
[InChIKey]

AXTADRUCVAUCRS-UHFFFAOYSA-N
[SMILES]

N1(CCO)C(=O)C=CC1=O
[CAS DataBase Reference]

1585-90-6
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319
[Precautionary statements ]

P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22-36
[Safety Statements ]

26
[WGK Germany ]

3
[HS Code ]

2925.19.9100
Hazard InformationBack Directory
[Description]

1-(2-hydroxymethyl)-1-H-pyrrole-2,5-dione is a synthetic building block for adding an maleimide group with a hydroxyl handle. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.
[Uses]

1-(2-Hydroxy-ethyl)-pyrrole-2,5-dione is a substituted succinimide with antibacterial and cytotoxic activities.
[reaction suitability]

reagent type: cross-linking reagent
[Synthesis]

3A,4,7,7A-TETRAHYDRO-2-(2'-HYDROXYETHYL)-4,7-EPOXY-1H-ISOINDOLE-1,3(2H)-DIONE

32620-90-9

1-(2-HYDROXY-ETHYL)-PYRROLE-2,5-DIONE

1585-90-6

General procedure for the synthesis of N-(2-hydroxyethyl)maleimide (HEMI) from 3a,4,7,7a-tetrahydro-2-(2'-hydroxyethyl)-4,7-epoxy-1H-isoindole-1,3(2H)-dione (HEMI-A): 0.19 mol (40 g) of HEMI-A was mixed with 227 g of xylene and 0.005 g of methylhydroquinone ( MEHQ, as antioxidant) was mixed. The reaction was heated under nitrogen protection at reflux at 130 °C for 3 h and 15 min to convert HEMI-A to HEMI with a conversion of 98.7% and a reaction yield of about 98.7%. After completion of the reaction, the reactor was cooled to room temperature, the reaction mixture was filtered and the solid product was washed with 15 g of xylene. The washed solid was dried under vacuum to give 25.1 g of HEMI in 93% yield based on HEMI-A. The purity of HEMI was confirmed to be greater than 99% by 1H-NMR analysis. The mother liquor and wash liquor were combined and the total mass was determined to be 230.2 g, which contained 1.17 g of HEMI, which can be recovered or recycled as described above.

[References]

[1] Patent: WO2007/44169, 2007, A1. Location in patent: Page/Page column 10
[2] Dyes and Pigments, 2017, vol. 145, p. 518 - 527
[3] Organic Letters, 2011, vol. 13, # 16, p. 4364 - 4367
[4] Advanced Functional Materials, 2014, vol. 24, # 33, p. 5261 - 5268,8
[5] Journal of Controlled Release, 2018, vol. 285, p. 187 - 199
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