Sodium borohydride → 2-Phenylisobutyric acid

HRID 133684

Reaktionsgleichung

Reaktionsgleichung von HRID 133684
OC1(C(C2C=CC=CC=2)C2C=CC=CC=2)CCCCN1CCCC([C:13]1[CH:18]=[CH:17][C:16]([C:19]([CH3:24])([CH3:23])[C:20]([OH:22])=[O:21])=[CH:15][CH:14]=1)=O.[BH4-].[Na+]>CO>[CH3:24][C:19]([C:16]1[CH:17]=[CH:18][CH:13]=[CH:14][CH:15]=1)([CH3:23])[C:20]([OH:22])=[O:21]

Komponenten

4

Edukt 2

HCID 4311764Sodium borohydrideHCID 867606954-[4-(Hydroxydiphenylmethyl-1-piperidinyl]-1-oxobutyl]-alpha,alpha-dimethylphenylacetic acid

Produkt 1

HCID 132222-Phenylisobutyric acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

A mixture of 4-[4-[4-(hydroxydiphenylmethyl-1-piperidinyl]-1-oxobutyl]-α,α-dimethylphenylacetic acid, prepared in accordance with Example 12, and 300 mg of NaBH4 in 25 mL of CH3OH was stirred overnight at room temperature. The mixture was then concentrated in vacuo. The residue was partitioned between EtOAc and H2O. The aqueous portion was treated with concentrated HCl until pH 6, then extracted with EtOAc. The organics were concentrated in vacuo. The residue was dissolved in EtOAc, filtered, and concentrated in vacuo to an oil. The oil was dissolved in CH3OH and concentrated to a solid. The solid was slurried with EtOAc, filtered, and rinsed with EtOAc to afford 4-[4-[4-hydroxydiphenylmethyl)-1-piperidinyl]-1-hydroxybutyl]-α,α-dimethylphenylacetic acid.

Aufarbeitung

  1. concentrationThe mixture was then concentrated in vacuo
  2. customThe residue was partitioned between EtOAc and H2O
  3. additionThe aqueous portion was treated with concentrated HCl until pH 6
  4. extractionextracted with EtOAc
  5. concentrationThe organics were concentrated in vacuo
  6. dissolutionThe residue was dissolved in EtOAc
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo to an oil
  9. dissolutionThe oil was dissolved in CH3OH
  10. concentrationconcentrated to a solid
  11. filtrationfiltered
  12. washrinsed with EtOAc

Quellen und Nachweise

ORD-Eintrag
ord-a493c1fff8a5433bb01556ea8fd4ec99
Quelldatensatz
uspto-grants-2008_06
Patentnummer
US07390906B2

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