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Hydrochloric Acid → 4-N-Propylphenylacetic Acid

HRID 2405652
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2405652
[CH2:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]#N)=[CH:6][CH:5]=1)[CH2:2][CH3:3].Cl.S([O-])([O-])(=O)=[O:15].[Mg+2].[OH-:20].[Na+]>>[CH2:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]([OH:15])=[O:20])=[CH:6][CH:5]=1)[CH2:2][CH3:3]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 24083Sulfuric acid magnesium salt (1:1)HCID 195934792-(4-Propylphenyl)acetonitrile

Produkt 1

HCID 39362184-N-Propylphenylacetic AcidAusbeute 76 %

Versuchsvorschrift

2-(4-propylphenyl)acetonitrile (41.0 mg, 0.257 mmol) was dissolved in 1 mL of 30% aqueous sodium hydroxide solution and stirred under reflux condition for 4 hours. Upon completion of the reaction, the reaction solution was acidified by adding 3 mL of 10% aqueous hydrogen chloride solution and extracted with diethyl ether (3 mL×3). The organic layer thus obtained was treated with anhydrous magnesium sulfate to remove water. The precipitate was filtered out and the resulting solution was concentrated by distillation under reduced pressure and purified by column chromatography to obtain 34.8 mg (0.195 mmol, 76%) of the desired compound (balance unit of tag β).

Aufarbeitung

  1. temperatureunder reflux condition for 4 hours
  2. customUpon completion of the reaction
  3. extractionextracted with diethyl ether (3 mL×3)
  4. customThe organic layer thus obtained
  5. customto remove water
  6. filtrationThe precipitate was filtered out
  7. concentrationthe resulting solution was concentrated by distillation under reduced pressure
  8. custompurified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-05bbc437b4c344b78edfc8230fa8f191
Quelldatensatz
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08809012B2

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