Sodium borohydride → 5-Methyl-3-phenylhexan-2-ol

HRID 1446403Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1446403
[CH3:1][CH:2]([CH3:14])[CH2:3][CH:4]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:5](=[O:7])[CH3:6].[BH4-].[Na+]>CO>[CH3:1][CH:2]([CH3:14])[CH2:3][CH:4]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[CH:5]([OH:7])[CH3:6]

Komponenten

4

Edukt 2

HCID 4311764Sodium borohydrideHCID 131565125-Methyl-3-phenylhexan-2-one

Produkt 1

HCID 222704255-Methyl-3-phenylhexan-2-ol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

A solution of 66 mg (0.345 mmol) of 5-methyl-3-phenyl-2-hexanone in 1 mL MeOH was treated with 16 mg sodium borohydride. After 1.5 h, the reaction was quenched with 1.2 N HCl and concentrated. The residue was partitioned between EtOAc and water. The organic layer was washed with brine, dried and concentrated to yield the crude title compound which was used without purification. 1H NMR: (500 MHz, CDCl3): δ 0.88 (2d, 6H), 1.0-1.8 (m, 4H), 1.2 (d, 3H), 2.64 (m, 1H), 3.9 (m, 1H), 7.2-7.4 (m, 5H).

Aufarbeitung

  1. customthe reaction was quenched with 1.2 N HCl
  2. concentrationconcentrated
  3. customThe residue was partitioned between EtOAc and water
  4. washThe organic layer was washed with brine
  5. customdried
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-accfadecf8e942e5a1525fdd9979419f
Quelldatensatz
uspto-grants-2010_02
Patentnummer
US07667053B2

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