Methyl 4-(benzyloxy)-3,5-dichlorobenzoate → (4-Benzyloxy-3,5-dichlorophenyl)methanol

HRID 901143Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 901143
C[O:2][C:3](=O)[C:4]1[CH:9]=[C:8]([Cl:10])[C:7]([O:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[C:6]([Cl:19])[CH:5]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[CH2:12]([O:11][C:7]1[C:6]([Cl:19])=[CH:5][C:4]([CH2:3][OH:2])=[CH:9][C:8]=1[Cl:10])[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1

Komponenten

4

Edukt 2

HCID 16749549Methyl 4-(benzyloxy)-3,5-dichlorobenzoateHCID 21226445Aluminium lithium hydride

Produkt 1

HCID 16749116(4-Benzyloxy-3,5-dichlorophenyl)methanol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

A solution of 4-benzyloxy-3,5-dichloro-benzoic acid methyl ester (CAB02115, 7.20 g, 23.14 mmol) in THF (20 mL) was added slowly with a syringe to a suspension of lithium aluminium hydride (1.50 g, 39.5 mmol) in THF (40 mL). The reaction mixture was stirred for 30 minutes at room temperature and then carefully quenched by addition of 2N sodium hydroxide solution in water. After 20 minutes stirring the colour of the mixture turned from grey to white. The white precipitate was filtered off, the filtrate was dried over sodium sulphate and concentrated under reduced pressure. The residue was recrystallised from dichloromethane/hexane. Yield: 5.83 g (89%) white powder. 1H-NMR (400 MHz, CDCl3) δ=1.85 (t, J=5.9 Hz, 1H, —OH), 4.63 (d, J=5.9 Hz, 2H), 5.04 (s, 2H), 7.33 (s, 2H), 7.35-7.44 (m, 3H), 7.55-7.59 (m, 2H). 13C-NMR (100 MHz, CDCl3) δ=64.05, 75.03, 127.36, 128.70, 128.75, 129.91, 136.39; 138.64, 150.32.

Aufarbeitung

  1. customcarefully quenched by addition of 2N sodium hydroxide solution in water
  2. stirringAfter 20 minutes stirring the colour of the mixture
  3. filtrationThe white precipitate was filtered off
  4. dry with materialthe filtrate was dried over sodium sulphate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was recrystallised from dichloromethane/hexane

Quellen und Nachweise

ORD-Eintrag
ord-e3cad6ba7f404f8a8f1f57331cd5807e
Quelldatensatz
uspto-grants-2008_04
Patentnummer
US07361677B2

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