StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

4-Pentenoyl chloride → N,N'-Bis[2-(acetyloxy)-1-[(acetyloxy)-methyl]ethyl]-2,4,6-triiodo-5-[(1-oxo-4-pentenyl) amino]-1,3-benzenedicarboxamide

HRID 260540
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 260540
[C:1](Cl)(=[O:6])[CH2:2][CH2:3][CH:4]=[CH2:5].[C:8]([O:11][CH2:12][CH:13]([NH:19][C:20]([C:22]1[C:27]([I:28])=[C:26]([NH2:29])[C:25]([I:30])=[C:24]([C:31]([NH:33][CH:34]([CH2:40][O:41][C:42](=[O:44])[CH3:43])[CH2:35][O:36][C:37](=[O:39])[CH3:38])=[O:32])[C:23]=1[I:45])=[O:21])[CH2:14][O:15][C:16](=[O:18])[CH3:17])(=[O:10])[CH3:9]>CC(N(C)C)=O>[C:37]([O:36][CH2:35][CH:34]([NH:33][C:31]([C:24]1[C:25]([I:30])=[C:26]([NH:29][C:1](=[O:6])[CH2:2][CH2:3][CH:4]=[CH2:5])[C:27]([I:28])=[C:22]([C:20]([NH:19][CH:13]([CH2:12][O:11][C:8](=[O:10])[CH3:9])[CH2:14][O:15][C:16](=[O:18])[CH3:17])=[O:21])[C:23]=1[I:45])=[O:32])[CH2:40][O:41][C:42](=[O:44])[CH3:43])(=[O:39])[CH3:38]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 42284934-Pentenoyl chlorideHCID 11766168N,N'-Bis[2-(acetyloxy)-1-[(acetyloxy)methyl]ethyl]-5-amino-2,4,6-triiodo-1,3-benzenedicarboxamide

Produkt 1

HCID 10373691N,N'-Bis[2-(acetyloxy)-1-[(acetyloxy)-methyl]ethyl]-2,4,6-triiodo-5-[(1-oxo-4-pentenyl) amino]-1,3-benzenedicarboxamideAusbeute 89 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 31374DimethylacetamideLösungsmittel

Versuchsvorschrift

4-Pentenoyl chloride (11.9 g, 100 mmol) was added to a stirred solution of N,N'-bis-[2-(acetyloxy)-1-[(acetyloxy)-methyl]ethyl]-5-amino-2,4,6 -triiodo-1,3-benzenedicarboxamide (47.75 g, 50 mmol) in dimethylacetamide (400 mL) at room temperature and the mixture was stirred for 16 hours. Dimethylacetamide was removed in vacuo and the residue dissolved in ethyl acetate (600 ml). The solution was washed with aqueous sodium bicarbonate (10%, 2×150 mL) and with water (2×100 mL) and brine (150 mL). The organic layer was dried and the solvent removed to obtain the crude product as an off-white solid. Further purification by crystallization from a mixture of acetone (250 mL) and hexane (75 mL) afforded the title A compound (42.5 g), m.p. 162°-64°. TLC: Rf 0.55 in ethyl acetate. Mass Spectrum: m/z 956 (M+H)+, 830, 653.

Aufarbeitung

  1. customDimethylacetamide was removed in vacuo
  2. dissolutionthe residue dissolved in ethyl acetate (600 ml)
  3. washThe solution was washed with aqueous sodium bicarbonate (10%, 2×150 mL) and with water (2×100 mL) and brine (150 mL)
  4. customThe organic layer was dried
  5. customthe solvent removed
  6. customto obtain the crude product as an off-white solid
  7. customFurther purification
  8. customby crystallization
  9. additionfrom a mixture of acetone (250 mL) and hexane (75 mL)

Quellen und Nachweise

ORD-Eintrag
ord-a227adb5584347019e9cf0455f838307
Quelldatensatz
uspto-grants-1996_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05527926

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion