Hydrochloric Acid → (R)-4-chloro-1-(3,5-dimethylphenyl)-3-methylbutan-1-one

HRID 1275052

Reaktionsgleichung

Reaktionsgleichung von HRID 1275052
[CH3:1][C:2]1[CH:3]=[C:4]([CH:14]=[C:15]([CH3:17])[CH:16]=1)[C:5]([C@H:7]1[CH:11]([CH3:12])[CH2:10]OC1=O)=[O:6].[ClH:18].C(=O)(O)[O-].[Na+]>>[Cl:18][CH2:10][C@H:11]([CH3:12])[CH2:7][C:5]([C:4]1[CH:3]=[C:2]([CH3:1])[CH:16]=[C:15]([CH3:17])[CH:14]=1)=[O:6]

Komponenten

4

Edukt 3

HCID 313Hydrochloric AcidHCID 516892Sodium Bicarbonate2×HCID 53860757(R)-3-(3,5-dimethylbenzoyl)-4-methyldihydrofuran-2-one

Produkt 1

HCID 53672991(R)-4-chloro-1-(3,5-dimethylphenyl)-3-methylbutan-1-one

Versuchsvorschrift

To a solution of (R)-3-(3,5-dimethylbenzoyl)-4-methyldihydrofuran-2-one (2.42 g in 15 mL dioxane) was added 15 mL conc. hydrochloric acid and the mixture heated to reflux on an oil bath. After one hour, the reaction was poured into cold, saturated aqueous sodium bicarbonate. Additional solid sodium bicarbonate was added until all acid was neutralized. This was then extracted with ethyl acetate, washed with brine. Concentration in vacuo provided the title compound (2.12 g).

Aufarbeitung

  1. temperaturethe mixture heated
  2. temperatureto reflux on an oil bath
  3. extractionThis was then extracted with ethyl acetate
  4. washwashed with brine
  5. concentrationConcentration in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-cf1f0c0ff88543d3a202ae41266ed2fc
Quelldatensatz
uspto-grants-2000_12
Patentnummer
US06159975

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