Triacetoxyperiodinane → [5-Methoxy-2-(2-oxo-butyl)-phenyl]-carbamic acid t-butyl Ester

HRID 985276Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 985276
CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.[C:23]([O:27][C:28](=[O:43])[NH:29][C:30]1[CH:35]=[C:34]([O:36][CH3:37])[CH:33]=[CH:32][C:31]=1[CH2:38][CH:39]([OH:42])[CH2:40][CH3:41])([CH3:26])([CH3:25])[CH3:24]>C1COCC1>[C:23]([O:27][C:28](=[O:43])[NH:29][C:30]1[CH:35]=[C:34]([O:36][CH3:37])[CH:33]=[CH:32][C:31]=1[CH2:38][C:39](=[O:42])[CH2:40][CH3:41])([CH3:25])([CH3:24])[CH3:26]

Komponenten

4

Versuchsvorschrift

To a solution of Dess-Martin reagent (2.82 g, 6.68 mmole) in 80 ml THF cooled at 0° C. was added [2-(2-hydroxy-butyl)-5-methoxy-phenyl]-carbamic acid t-butyl ester 73a (1.64 g, 5.57 mmole) in 20 ml THF. The reaction mixture was stirred and warmed to room temperature for 2 h, quenched with half saturated NaHCO3, extracted with EtOAc. The organic layer was dried over MgSO4 and concentrated. The residue was purified by flash column chromatography (10-15% EtOAc in hexane) to give colorless oil (1.36 g, 84%). 1H NMR (CDCl3) δ7.67 (1H, bs), 7.48 (1H, s), 6.99-7.03 (1H, m), 6.56-6.60 (1H, m), 3.79 (3H, s), 3.59 (2H, s), 2.53-2.61 (2H, q, J=7.2 Hz), 1.51 (9H, s), 1.02 (3H, t, J=7.2 Hz). ESIMS (MNa+): 316.10.

Aufarbeitung

  1. customquenched with half saturated NaHCO3
  2. extractionextracted with EtOAc
  3. dry with materialThe organic layer was dried over MgSO4
  4. concentrationconcentrated
  5. customThe residue was purified by flash column chromatography (10-15% EtOAc in hexane)

Quellen und Nachweise

ORD-Eintrag
ord-38195f8b34454ee9a60434b253d53d76
Quelldatensatz
uspto-grants-2005_03
Patentnummer
US06869962B2

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