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

4-Hydroxybenzaldehyde → 4-(3-(Diethylamino)propoxy)benzaldehyde

HRID 17651
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 17651
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1.C([O-])([O-])=O.[Cs+].[Cs+].S([O-])(=O)(=O)C.[CH2:21]([N:23]([CH2:28][CH3:29])[CH2:24][CH2:25][CH2:26]O)[CH3:22].CS(Cl)(=O)=O>CS(C)=O>[CH2:21]([N:23]([CH2:28][CH3:29])[CH2:24][CH2:25][CH2:26][O:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1)[CH3:22]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 1264-HydroxybenzaldehydeHCID 10796Cesium carbonateHCID 121593-(Diethylamino)-1-propanolHCID 31297Methanesulfonyl chlorideHCID 85257Methanesulfonate

Produkt 1

HCID 176070434-(3-(Diethylamino)propoxy)benzaldehyde

Reagenzien, Katalysatoren, Lösungsmittel

1
HCID 679Dimethyl SulfoxideLösungsmittel

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

To a stirred solution of 4-hydroxybenzaldehyde (20 mmol) in DMSO (80 mL) at rt, solid Cs2CO3 (50 mmol) was added. The mesylate prepared from 3-diethylamino-1-propanol and methanesulfonyl chloride, General Procedure P2 (30 mmol) was added to the reaction mixture and heated to 90° C. until the reaction was complete. After cooling to rt, the reaction was quenched by cold H2O (100 mL), and the resulting mixture was extracted with EtOAc (3×100 mL). The combined EtOAc extracts were washed with brine (3×50 mL) and dried (anhydrous Na2SO4). The solvent was removed in vacuo, and the crude product was purified by silica gel column chromatography (eluting with 10% MeOH in DCM+0.5% Et3N) to afford 4-(3-diethylaminopropoxy)benzaldehyde.

Aufarbeitung

  1. additionwas added to the reaction mixture
  2. temperatureAfter cooling to rt
  3. customthe reaction was quenched by cold H2O (100 mL)
  4. extractionthe resulting mixture was extracted with EtOAc (3×100 mL)
  5. washThe combined EtOAc extracts were washed with brine (3×50 mL)
  6. dry with materialdried (anhydrous Na2SO4)
  7. customThe solvent was removed in vacuo
  8. customthe crude product was purified by silica gel column chromatography (eluting with 10% MeOH in DCM+0.5% Et3N)

Quellen und Nachweise

ORD-Eintrag
ord-db5bf796934549268433edbace0a4a79
Quelldatensatz
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07737285B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion