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Chemical Structure| 32620-90-9 Chemical Structure| 32620-90-9

Structure of 32620-90-9

Chemical Structure| 32620-90-9

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Product Details of [ 32620-90-9 ]

CAS No. :32620-90-9
Formula : C10H11NO4
M.W : 209.20
SMILES Code : O=C1N(CCO)C(C2C(O3)C=CC3C12)=O
MDL No. :MFCD08274857
InChI Key :ISKZEUQQPPVQNW-UHFFFAOYSA-N
Pubchem ID :12193800

Safety of [ 32620-90-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362

Application In Synthesis of [ 32620-90-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 32620-90-9 ]

[ 32620-90-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 32620-90-9 ]
  • [ 1585-90-6 ]
YieldReaction ConditionsOperation in experiment
93% With 1,4-dimethoxybezene; In xylene; at 130℃; for 3.25h;Heating / reflux; A 0.19 mol (4Og) sample of the HEMI-A from above was mixed with 227g of xylene and 0.005g methyl hydroquinone (MEHQ), an antioxidant. After heating under reflux and nitrogen sparging for 3 hours 15 minutes at 1300C, the conversion of HEMI-A to HEMI reached 98.7% and the reaction yield was determined to be approximately 98.7%. The reactor was cooled to room temperature, and the cooled reaction product was filtered at room temperature, and the filtered solids were washed with 15g of xylenes. The washed solids were dried under vacuum, and 25. Ig of HEMI, a 93% yield based on the HEMI-A, was obtained. The purity of the HEMI was determined to be greater than 99% by H-NMR. It was EPO <DP n="13"/>also determined that the mother liquor and wash liquid was combined and determined to weigh 230.2g and contain 1.17g of HEMI, which could be recovered as described above, or recycled.
81% In toluene; for 7h;Reflux; The synthesis of 1-(2-Hydroxyethyl)-1H-pyrrole-2,5-dione (5) was carried out following methods reported in a previous publication [43]. In a 50mL round-bottom flask adapted with a flux condenser and magnetic stirring, the intermediate 4 (2.30g, 10.99mmol) was combined with toluene (30mL). The reaction was refluxed for 7h. The resulting mixture was immediately filtered, and the product crystallised from toluene in 81% yield (1.25g, 8.87mmol). 1H-NMR (400MHz, DMSO-d6) delta 7.01 (s, 2H), 4.78 (br, 1H), 3.46 (br, 4H); 13C-NMR (100MHz, DMSO-d6) delta 171.1, 134.5, 57.9, 39.9.
In toluene; for 12h;Reflux; Inert atmosphere; General procedure: N-(2-hydroxyethyl)maleimide (Mal-OH) was prepared according to a previously reported method [3, 34]. Firstly, 30.0 g maleic anhydride (306mmol)was dissolved in toluene and 22.4 ml furan (309mmol) was slowly injected into the solution via syringe. After the mixture stirred for 24 h at room temperature, the reaction was stopped and the white crystals were precipitated from the mixture, collected and washed with toluene. The white powder was dried in a vacuum oven to prepare furan-protected maleic anhydride. Secondly, the furan-protected maleic anhydride(4.98 g, 30mmol) was suspended in methanol and stirred at 0 C. Then1.8 ml of ethanolamine (30mmol) was added dropwise to the solution,stirred and refluxed at 80 C for 24 h. Then the reaction mixture was cooled to 0 C, the product was crystallized from the mixture and collected to obtain furan-protected N-(2-hydroxyethyl)-maleimide. Finally,furan-protected N-(2-hydroxyethyl)-maleimide (2.1 g, 10mmol) in 10 ml toluene was stirred and refluxed under nitrogen for 12 h. The reaction mixture was hot filtered, and the filtrate was stored at 4 C overnight.The product crystallized from the mixture, then collected, dried under vacuum for 24 h to obtain N-(2-hydroxyethyl)-maleimide (Mal-OH)
 

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