反応 #1673257

ord-1a9ab788dca54fbe89adb8b98b3c1663

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGAfter stirring for an additional 5 mins the reaction mixture
  2. 2
    抽出extracted with methylene chloride
  3. 3
    その他The extracts are dried
  4. 4
    その他evaporated under reduced pressure
  5. 5
    その他The crude product is chromatographed on silica-gel
  6. 6
    洗浄Elution with 30% acetone-hexane

実験手順

A solution of 1-hexyl-3-formyl-4-methoxy-6-methyl-2(1H)-quinolinone (Step (2) of Example 1, 10 g) in methanol (80 ml) was cooled in an ice-bath and stirred while adding, in small lots, solid sodium borohydride (0.5 g). After stirring for an additional 5 mins the reaction mixture was carefully diluted with water and extracted with methylene chloride. The extracts are dried and evaporated under reduced pressure. The crude product is chromatographed on silica-gel. Elution with 30% acetone-hexane gave 1-hexyl-3-hydroxymethyl-4-methoxy-6-methyl-2(1H)-quinolinone. That the expected product was obtained was confirmed by the spectral data: MS: m/e 303 (M.+); NMR (CDCl3): δ4.0 (s, H, OCH3), 4.75 (d, 2H, CH2O).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05942522uspto-grants-1999_08