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Methanol → Methyl 2-(3-methoxy-4-nitrophenyl)acetate

HRID 1019749
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1019749
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:12][C:13]([OH:15])=[O:14])[CH:6]=[CH:7][C:8]=1[N+:9]([O-:11])=[O:10].[CH3:16]O>OS(O)(=O)=O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:12][C:13]([O:15][CH3:16])=[O:14])[CH:6]=[CH:7][C:8]=1[N+:9]([O-:11])=[O:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 887MethanolHCID 16755859(3-Methoxy-4-nitrophenyl)acetic acid

Produkt 1

HCID 67467853Methyl 2-(3-methoxy-4-nitrophenyl)acetateAusbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1118Sulfuric AcidKatalysator

Versuchsvorschrift

A solution of 2-(3-methoxy-4-nitrophenyl)acetic acid (4.6 g, 21.78 mmol) and concentrated H2SO4 (2 drops) in methanol (200 mL) was heated to reflux for 3 hours. The mixture was allowed to cool to room temperature then the solvents were removed under reduced pressure. The residue was partitioned between water (100 mL) and EtOAc (100 mL), then the separated organic layer was washed with sodium bicarbonate solution (100 mL), brine (200 mL), dried (Na2SO4) and evaporated under reduced pressure to give the title compound (4.5 g, 92%) as a solid.

Aufarbeitung

  1. temperatureto reflux for 3 hours
  2. customthe solvents were removed under reduced pressure
  3. customThe residue was partitioned between water (100 mL) and EtOAc (100 mL)
  4. washthe separated organic layer was washed with sodium bicarbonate solution (100 mL), brine (200 mL)
  5. dry with materialdried (Na2SO4)
  6. customevaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-b89fb5257c694111a67f4d04bceac5a5
Quelldatensatz
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08716287B2

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