Reaktion #1780

ord-997799bff2054cbcbc860fbe74d39dc5

Reaktionsgleichung

Cc1cnc2c(c1)C(=O)CC(C)(C)C2
5,6,7,8-tetrahydro-3,7,7-trimethylquinoline-5-one
[BH4-].[Na+]
NaBH4
Cc1cnc2c(c1)C(O)CC(C)(C)C2
5,6,7,8-tetrahydro-3,7,7-trimethylquinoline-5-ol

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was removed under reduced pressure
  2. 2
    Sonstigethe crude oil that was chromatographed on a silica gel column
  3. 3
    Waschenhexanes and eluted with same
  4. 4
    Sonstigethe solvent was removed under reduced pressure

Vorschrift

A stirred solution of 5,6,7,8-tetrahydro-3,7,7-trimethylquinoline-5-one (240 mg, 1.3 mmol) in MeOH (6.5 mL) was cooled to 0° C. under Argon and treated with NaBH4 (48 mg, 1.3 mmol). The reaction was stirred over 14 h and allowed to warm to ambient temperature. The solvent was removed under reduced pressure and the crude oil that was chromatographed on a silica gel column packed in 95:5 EtOAc:hexanes and eluted with same. The appropriate fractions were combined and the solvent was removed under reduced pressure to give 5,6,7,8-tetrahydro-3,7,7-trimethylquinoline-5-ol.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726172uspto-grants-1998_03