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Methanol → HCID 11299024, Verbindung

HRID 546635
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 546635
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]([CH3:15])([CH3:14])[C:11]([OH:13])=[O:12])=[CH:6][CH:5]=1)([O-:3])=[O:2].S(=O)(=O)(O)O.[CH3:21]O>>[CH3:14][C:10]([C:7]1[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=1)([CH3:15])[C:11]([O:13][CH3:21])=[O:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 7818982-Methyl-2-(4-nitrophenyl)propanoic acid

Produkt 1

HCID 11299024HCID 11299024, Verbindung

Versuchsvorschrift

To a solution of 5 g of 2-(4-nitrophenyl)-2-methylpropionic acid in 40 mL of methanol, under argon, are added 4 mL of sulphuric acid. The reaction medium is heated at reflux for 3 hours and concentrated under reduced pressure. The residue is taken up in a mixture of ice-water and dichloromethane, the phases are separated and the organic phase is dried over magnesium sulphate and filtered. The filtrate is concentrated under reduced pressure to give 5.18 g of methyl 2-methyl-2-(4-nitrophenyl)propanoate in the form of a pale yellow solid, the characteristics of which are as follows:

Aufarbeitung

  1. temperatureThe reaction medium is heated
  2. temperatureat reflux for 3 hours
  3. concentrationconcentrated under reduced pressure
  4. additionThe residue is taken up in a mixture of ice-water and dichloromethane
  5. customthe phases are separated
  6. dry with materialthe organic phase is dried over magnesium sulphate
  7. filtrationfiltered
  8. concentrationThe filtrate is concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-66f9845d7a264659b06cd4e4c8401788
Quelldatensatz
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07935819B2

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