Pyridine → 2-Ethylcarbonate Ethylmaleimide

HRID 1268089Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1268089
[OH:1][CH2:2][CH2:3][C:4]1[C:5]([NH:7][C:8](=[O:10])[CH:9]=1)=[O:6].N1C=CC=CC=1.Cl[C:18]([O:20][CH2:21][CH3:22])=[O:19]>C1COCC1>[CH2:3]([C:4]1[C:5]([NH:7][C:8](=[O:10])[CH:9]=1)=[O:6])[CH3:2].[CH3:22][CH2:21][O:20][C:18](=[O:1])[OH:19]

Komponenten

5

Edukt 3

HCID 1049PyridineHCID 10928Ethyl chloroformateHCID 22337974Hydroxy ethylmaleimide

Produkt 1

HCID 685376102-Ethylcarbonate Ethylmaleimide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

Hydroxy ethylmaleimide (29.87 g, 0.212 moles) and pyridine (16.7 g, 0.212 moles) were dissolved in THF (170 mL) and the solution was stirred at room temperature. Ethyl chloroformate (22.97 g, 0.212 moles) was added dropwise and stirred for 90 minutes. The pyridine salt was filtered off and the solution was combined with 200 mL of a 1N HCl solution. The product was extracted with methylene chloride and washed with a 1N HCl solution followed by water and then dried over magnesium sulfate. The red solution was concentrated and the red crystals purified by sublimation yielding white crystals, m.p. 52° C. (34.76 g, 77.04%). 1H-NMR (CDCl3), δ, ppm): 1.26-1.34 (3H, —CH3, t), 3.81-3.87 (2H—NCH2—, t), 4.14-4.25 (2H, δ-CH2OC═O, q), 4.25-4.30 (2H, β-CH2O—, t), 6.74 (2H, —CH═CH—, s). 13C-NMR (CDCl3, δ, ppm): 14.2 (1C, —CH3), 36.8 (1C, —NCH2—), 64.3 (1C, δ-CH2O), 64.5 (1C, β-CH2—), 134.4 (2C, —CH═CH—), 154.9 (1C, O(C═O)O), 170.4 (2C, —C═O).

Aufarbeitung

  1. stirringstirred for 90 minutes
  2. filtrationThe pyridine salt was filtered off
  3. extractionThe product was extracted with methylene chloride
  4. washwashed with a 1N HCl solution
  5. dry with materialdried over magnesium sulfate
  6. concentrationThe red solution was concentrated
  7. customthe red crystals purified by sublimation
  8. customyielding white crystals, m.p. 52° C. (34.76 g, 77.04%)

Quellen und Nachweise

ORD-Eintrag
ord-f6bfdd770dec44b6a3d4178d0d70ae25
Quelldatensatz
uspto-grants-2003_04
Patentnummer
US06555593B1

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