Water → 5,7-Dimethylchroman-2-one

HRID 1761656

Reaktionsgleichung

Reaktionsgleichung von HRID 1761656
C[C:2]([C:4]1[CH:13]=[CH:12][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]=1O)=O.C12CC3CC(CC(C3)C1=[O:25])C2.N1CCCC1.[OH2:31]>C1(C)C=CC=CC=1>[CH3:7][C:6]1[CH:5]=[C:4]([CH3:2])[CH:13]=[C:12]2[C:11]=1[CH2:10][CH2:9][C:8](=[O:25])[O:31]2

Komponenten

6

Versuchsvorschrift

A mixture of 1-hydroxy-2-acetonaphthone (10.1 g), (1A), adamantanone (9 g) and pyrrolidine (10 cm3) in toluene (300 cm3) was boiled (10 hours) and water separated. The yellow reaction mixture turned first crimson and then dark brown. Toluene was removed under reduced pressure and the residual enamine crystallised from acetone as discoloured crystals (8 g). The enamine (2) (10 g) was treated with conc. hydrochloric acid (1 cm3) in methanol (200 cm3). The crimson solution was evaporated and the residual dark oil crystallised from acetone, yielding the chromanone (3) (8.4 g) as yellow needles. The chromanone (0.5 g) was reduced by sodium borohydride (0.5 g) in methanol to yield the chromanol (4) (0.32 g) which was heated with anhydrous copper sulphate to give HC7 (formula (5) R=H) (0.28 g) as a discoloured solid which was decolourised with activated charcoal and recrystallised from acetone.

Aufarbeitung

  1. customseparated
  2. customToluene was removed under reduced pressure
  3. customthe residual enamine crystallised from acetone as discoloured crystals (8 g)
  4. additionThe enamine (2) (10 g) was treated with conc. hydrochloric acid (1 cm3) in methanol (200 cm3)
  5. customThe crimson solution was evaporated
  6. customthe residual dark oil crystallised from acetone

Quellen und Nachweise

ORD-Eintrag
ord-9727f45321f34d7bb00e7446f2686b27
Quelldatensatz
uspto-grants-1989_05
Patentnummer
US04826977

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