Methyl 4-methoxyphenylacetate → 4-Methoxyphenylacetaldehyde

HRID 30333

Reaktionsgleichung

Reaktionsgleichung von HRID 30333
C[O:2][C:3](=O)[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([O:11][CH3:12])=[CH:7][CH:6]=1.[H-].C([Al+]CC(C)C)C(C)C>C1(C)C=CC=CC=1>[CH3:12][O:11][C:8]1[CH:9]=[CH:10][C:5]([CH2:4][CH:3]=[O:2])=[CH:6][CH:7]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To a stirred solution of (4-Methoxy-phenyl)-acetic acid methyl ester (18.0 g, 100 mmol) in anhydrous toluene (200 mL) cooled to −78° C. under N2 was added diisobutylaluminum hydride (DIBAL, 1.0 M in toluene, 150 mL, 150 mmol) over a period of 10-15 minutes. The mixture was stirred at −78° C. for an additional 2 h. The reaction was quenched by the slow addition of MeOH, followed by the introduction of 10% Rochelle's Salt. The suspension was diluted with EtOAc and stirred at room temperature for 1 h. The EtOAc layer was set aside and the aqueous layer was extracted with EtOAc(2×). The combined organic layers were combined and dried over Na2SO4 and filtered. The solution was concentrated under vacuum to yield 12.0 g (100%) of the title aldehyde as a yellow viscous semisolid, which was used in the next step without purification. LC/MS (APCI, ES, M+H=151).

Aufarbeitung

  1. customThe reaction was quenched by the slow addition of MeOH
  2. additionThe suspension was diluted with EtOAc
  3. stirringstirred at room temperature for 1 h
  4. extractionthe aqueous layer was extracted with EtOAc(2×)
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationThe solution was concentrated under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-06f62880249045769a4db217abe68a7c
Quelldatensatz
uspto-grants-2008_09
Patentnummer
US07423061B2

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