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Methanol → Methyl 3-amino-4-propylbenzoate

HRID 1072879
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1072879
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=1[CH2:13][CH2:14][CH3:15])[C:7]([OH:9])=[O:8])([O-])=O.S(=O)(=O)(O)O.[CH3:21]O>[Pd]>[NH2:1][C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=1[CH2:13][CH2:14][CH3:15])[C:7]([O:9][CH3:21])=[O:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 155216373-Nitro-4-propylbenzoic acid

Produkt 1

HCID 22387873Methyl 3-amino-4-propylbenzoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 23938PalladiumKatalysator

Versuchsvorschrift

To 3-nitro-4-propylbenzoic acid (31.0 g) were added sulfuric acid (1.0 g) and methanol (300 ml) and the mixture was heated under reflux for 24 hr. After cooling, 5% Pd-C (0.60 g) was added to the reaction mixture and the mixture was stirred under a hydrogen atmosphere (normal pressure) for 6 hr. The reaction mixture was filtered through Celite and concentrated. To the residue was added a saturated aqueous sodium hydrogencarbonate solution, and the mixture was extracted with toluene. The toluene layer was dried over sodium sulfate and concentrated to give the object compound (28.7 g) as an brown oil.

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 24 hr
  3. temperatureAfter cooling
  4. filtrationThe reaction mixture was filtered through Celite
  5. concentrationconcentrated
  6. additionTo the residue was added a saturated aqueous sodium hydrogencarbonate solution
  7. extractionthe mixture was extracted with toluene
  8. dry with materialThe toluene layer was dried over sodium sulfate
  9. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-b963fd9283674be3926408622d4e3b94
Quelldatensatz
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06911469B2

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