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Sodium Hydroxide → 4-Methyl-2-phenylpentanoic acid

HRID 902746
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 902746
C[C:2]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)([CH2:6][C:7]([CH3:9])=[CH2:8])[C:3]([OH:5])=[O:4].[OH-].[Na+]>O>[C:10]1([CH:2]([CH2:6][CH:7]([CH3:9])[CH3:8])[C:3]([OH:5])=[O:4])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 69253057Methyl 2-phenyl-4-methyl-4-pentenoic Acid

Produkt 1

HCID 2365774-Methyl-2-phenylpentanoic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

A solution of methyl 2-phenyl-4-methyl-4-pentenoic acid (850 mg, 4.15 mmole) in 10 mL of MeOHwas treated with 5 mL of 2.5N NaOH and heated to 50° for 30 minutes. The reaction was cooled, diluted with H2O and washed with Et2O. The aqueous phase was acified, and extracted with CH2Cl2. The extracts were washed with H2O, dried and the solvent removed. The residue was dissolved in 25 mL of EtOAc, and hydrogenated over a 10% Pd/C catalyst, at 1 atmosphere H2 pressure, for 2 hours. The catalyst was filtered and the solvent removed and gave the titled compound, 647 mg (81%). MS (ESI) 193 (MH+)

Aufarbeitung

  1. temperatureheated to 50° for 30 minutes
  2. temperatureThe reaction was cooled
  3. washwashed with Et2O
  4. extractionextracted with CH2Cl2
  5. washThe extracts were washed with H2O
  6. customdried
  7. customthe solvent removed
  8. dissolutionThe residue was dissolved in 25 mL of EtOAc
  9. filtrationThe catalyst was filtered
  10. customthe solvent removed

Quellen und Nachweise

ORD-Eintrag
ord-963f3a8ff95a4f48950097331f079fa7
Quelldatensatz
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07365085B2

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