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Dimethyl Sulfate → 2,3-Dimethoxy-6-nitrobenzaldehyde

HRID 580036
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 580036
[K].[OH:2][C:3]1[C:10]([O:11][CH3:12])=[CH:9][CH:8]=[C:7]([N+:13]([O-:15])=[O:14])[C:4]=1[CH:5]=[O:6].[C:16](=O)([O-])[O-].[K+].[K+].COS(OC)(=O)=O.[K]>CC(C)=O>[CH3:16][O:2][C:3]1[C:10]([O:11][CH3:12])=[CH:9][CH:8]=[C:7]([N+:13]([O-:15])=[O:14])[C:4]=1[CH:5]=[O:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6497Dimethyl Sulfate2×HCID 11430Potassium CarbonateHCID 5462222PotassiumHCID 867411922-Hydroxy-3-methoxy-6-nitrobenzaldehyde potassium salt

Produkt 1

HCID 71721272,3-Dimethoxy-6-nitrobenzaldehydeAusbeute 80 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 180
Acetone
Lösungsmittel

Versuchsvorschrift

2-Hydroxy-3-methoxy-6-nitrobenzaldehyde potassium salt was slurried in acetone (500 mL) containing potassium carbonate (50 g) and the suspension was treated with dimethylsulfate (18.5 mL) and heated to reflux for one hour. An additional aliquot (18.5 mL) of dimethylsulfate was then added and the mixture was heated overnight. After 24 hours the red color of the potassium salt was virtually absent. The salts were removed by filtration, the filtrate was concentrated and the residue was recrystallized from isopropanol to give the title compound 40.0 g (80% from 3) mp 109°-110° C.

Aufarbeitung

  1. temperatureheated
  2. temperatureto reflux for one hour
  3. temperaturethe mixture was heated overnight
  4. customThe salts were removed by filtration
  5. concentrationthe filtrate was concentrated
  6. customthe residue was recrystallized from isopropanol

Quellen und Nachweise

ORD-Eintrag
ord-fdb1135aa64f479b9d5ffa1f9f79fafb
Quelldatensatz
uspto-grants-1988_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04751304

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