反応 #1673257
ord-1a9ab788dca54fbe89adb8b98b3c1663
反応方程式
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1workup.STIRRINGAfter stirring for an additional 5 mins the reaction mixture
- 2抽出extracted with methylene chloride
- 3その他The extracts are dried
- 4その他evaporated under reduced pressure
- 5その他The crude product is chromatographed on silica-gel
- 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).