Ammonium Chloride → 2-benzyloxy-N-[1-(3,5-dichlorophenylthio)-3-methyl-2-oxobutyl]-N-methylacetamide

HRID 1416010

Reaktionsgleichung

Reaktionsgleichung von HRID 1416010
[CH2:1]([O:8][CH2:9][C:10]([N:12]([CH3:19])[CH2:13][C:14](=[O:18])[CH:15]([CH3:17])[CH3:16])=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([Li])CCC.[Cl:25][C:26]1[CH:27]=[C:28]([S:33]C2C=C(Cl)C=C(Cl)C=2)[CH:29]=[C:30]([Cl:32])[CH:31]=1.[Cl-].[NH4+]>O1CCCC1.CCCCCC>[CH2:1]([O:8][CH2:9][C:10]([N:12]([CH:13]([S:33][C:28]1[CH:29]=[C:30]([Cl:32])[CH:31]=[C:26]([Cl:25])[CH:27]=1)[C:14](=[O:18])[CH:15]([CH3:17])[CH3:16])[CH3:19])=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

7

Edukt 4

HCID 25517Ammonium ChlorideHCID 211871173,5-DichlorophenylsulfideHCID 221309122-benzyloxy-N-methyl-N-(3-methyl-2-oxobutyl)acetamideHCID 178418339Butyllithium

Produkt 1

HCID 221306862-benzyloxy-N-[1-(3,5-dichlorophenylthio)-3-methyl-2-oxobutyl]-N-methylacetamideAusbeute 47 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8028TetrahydrofuranLösungsmittel2×HCID 8058HexaneLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

In 2 ml of dry tetrahydrofuran was dissolved 100 mg (0.4 mmol )of 2-benzyloxy-N-methyl-N-(3-methyl-2-oxobutyl)acetamide (18a'), and there was added 223 μl (0.4 mmol)of n-butyllithium (1.7 M hexane solution)with stirring at -78° C. over 10 minutes. After stirring at -78° C. for 1 hour, and a tetrahydrofuran solution (1 ml)of 135 mg (0.4 mmol)of 3,5-dichlorophenylsulfide was added thereto over 10 minutes. After 30 minutes, the temperature was raised up to room temperature, a saturated aqueous ammonium chloride solution was added, and the mixture was extracted with ethyl acetate ester. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The crude product was purified by silica gel chromatography (hexane/ethyl acetate 5:1)to give 79 mg of 2-benzyloxy-N-[1-(3,5-dichlorophenylthio)-3-methyl-2-oxobutyl]-N-methylacetamide (20)(yield 47%).

Aufarbeitung

  1. stirringAfter stirring at -78° C. for 1 hour
  2. waitover 10 minutes
  3. waitAfter 30 minutes
  4. temperaturethe temperature was raised up to room temperature
  5. extractionthe mixture was extracted with ethyl acetate ester
  6. washThe extract was washed with saturated brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe crude product was purified by silica gel chromatography (hexane/ethyl acetate 5:1)to

Quellen und Nachweise

ORD-Eintrag
ord-eff25180eddf4bb88481975cbe0a97d5
Quelldatensatz
uspto-grants-1999_06
Patentnummer
US05910506

Verknüpfte Notizen

Wird geladen…