2-(2,5-Difluoro-4-nitrophenyl)-2-isobutylmalonic acid diethyl ester → 2-(2,5-Difluoro-4-nitro-phenyl)-4-methyl-pentanoic acid

HRID 1512375Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1512375
C([O:3][C:4](=[O:26])[C:5]([C:15]1[CH:20]=[C:19]([F:21])[C:18]([N+:22]([O-:24])=[O:23])=[CH:17][C:16]=1[F:25])([CH2:11][CH:12]([CH3:14])[CH3:13])C(OCC)=O)C>CC(O)=O.O.CCO>[F:25][C:16]1[CH:17]=[C:18]([N+:22]([O-:24])=[O:23])[C:19]([F:21])=[CH:20][C:15]=1[CH:5]([CH2:11][CH:12]([CH3:14])[CH3:13])[C:4]([OH:26])=[O:3]

Komponenten

3

Edukt 1

HCID 579955742-(2,5-Difluoro-4-nitrophenyl)-2-isobutylmalonic acid diethyl ester

Produkt 1

HCID 579955592-(2,5-Difluoro-4-nitro-phenyl)-4-methyl-pentanoic acidAusbeute 64,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 86584229Acetic acid ethanol waterLösungsmittel

Versuchsvorschrift

The above 2-(2,5-difluoro-4-nitrophenyl)-2-isobutylmalonic acid diethyl ester (57.0 g, 152.8 mmol) was dissolved in AcOH/H2O/EtOH (400 mL/120 mL/50 mL) and the reaction mixture was heated under reflux for 96 h. After cooling the solvent was evaporated under reduced pressure and water (200 mL) was added. The reaction mixture was extracted with EtOAc (3×100 mL), and the combined extracts were washed with water (3×100 mL), brine (100 mL) and dried (MgSO4). Evaporation of solvent under reduced pressure gave a yellow oil which crystallized on standing to yield 27 g of 2-(2,5-difluoro-4-nitro-phenyl)-4-methyl-pentanoic acid. Chromatography of the residual oil (Heptane-EtOAc gradient) gave an additional 3 g of product (72% combined yield). 1H NMR (300 MHz, CDCl3/TMS): δ 9.63 (br s, 1H), 7.82 (dd, J=8.8, 6.0 Hz, 1H), 7.38 (dd, J=11.0, 5.8 Hz, 1H), 4.14-4.08 (m, 1H), 2.05-1.95 (m, 1H), 1.76-1.66 (m, 1H), 1.52-1.43 (m, 1H), 0.95-0.92 (m, 6H); 13C NMR (75 MHz, CDCl3/TMS): δ 177.6, 158.2 (d, 1JCF=232.5 Hz), 150.9 (d, 1JCF=262.5 Hz), 136.0, 134.7, 119.0 (d, 2JCF=20.0, Hz), 113.1 (d, 2JCF=29.4 Hz), 41.7, 41.3, 26.0, 22.6, 21.9.

Aufarbeitung

  1. temperaturethe reaction mixture was heated
  2. temperatureunder reflux for 96 h
  3. temperatureAfter cooling the solvent
  4. customwas evaporated under reduced pressure and water (200 mL)
  5. additionwas added
  6. extractionThe reaction mixture was extracted with EtOAc (3×100 mL)
  7. washthe combined extracts were washed with water (3×100 mL), brine (100 mL)
  8. dry with materialdried (MgSO4)
  9. customEvaporation of solvent under reduced pressure
  10. customgave a yellow oil which
  11. customcrystallized

Quellen und Nachweise

ORD-Eintrag
ord-e2b70a1cb56c476dae147f21553975a2
Quelldatensatz
uspto-grants-2012_07
Patentnummer
US08217064B2

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