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

Methanol → 1-Methanesulfonyl-5-methoxy-phenylamine

HRID 418076
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 418076
[CH3:1][S:2]([C:5]1[CH:10]=[C:9]([N+]([O-])=O)[CH:8]=[C:7]([O:14][CH3:15])[CH:6]=1)(=[O:4])=[O:3].[Cl-].[NH4+:17].CO>[Zn].O>[CH3:1][S:2]([C:5]1([NH2:17])[CH:6]=[C:7]([O:14][CH3:15])[CH:8]=[CH:9][CH2:10]1)(=[O:4])=[O:3]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 887MethanolHCID 25517Ammonium ChlorideHCID 578630801-(Methanesulfonyl)-3-methoxy-5-nitrobenzene

Produkt 1

HCID 666496371-Methanesulfonyl-5-methoxy-phenylamineAusbeute 76 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23994ZincKatalysator
HCID 962
Water
Lösungsmittel
2×

Versuchsvorschrift

To a mixture of 1-methanesulfonyl-3-methoxy-5-nitro-benzene (1.5 g, 6.48 mmol), zinc dust (4.3 g, 64.87 mmol), and ammonium chloride (5.2 g, 97.31 mmol) were added methanol (20.32 mL) and water (9.9 mL) at room temperature. After addition of water, the reaction was exothermic. The suspension was stirred for 30 min and the reaction mixture was filtered through the Celite. The filter cake was washed with water and methanol. The filtrate was concentrated to remove methanol and the residue was extracted with ethyl acetate (2×50 mL). The combined extracts were washed with brine solution (100 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to isolate 1-methanesulfonyl-5-methoxy-phenylamine (1.0 g, 76%) as a light yellow solid: ES(+)-HRMS m/e calcd for C8H12NO3S (M+H)+ 202.0533, found 202.0532.

Aufarbeitung

  1. filtrationthe reaction mixture was filtered through the Celite
  2. washThe filter cake was washed with water and methanol
  3. concentrationThe filtrate was concentrated
  4. customto remove methanol
  5. extractionthe residue was extracted with ethyl acetate (2×50 mL)
  6. washThe combined extracts were washed with brine solution (100 mL)
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-e5198d1f0cc34967ab0f6e775fe13335
Quelldatensatz
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08093253B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion