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Methyl iodide → HCID 23116231, Verbindung

HRID 495198
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 495198
[CH2:1]([O:4][C:5]1[C:6]([CH2:38][CH3:39])=[C:7]([CH2:27][C:28]([N:30]([CH2:35][CH2:36][OH:37])[CH2:31][CH2:32][O:33][CH3:34])=[O:29])[C:8]([C:15](=[O:26])[C:16]2[CH:21]=[CH:20][C:19]([S:22]([CH3:25])(=[O:24])=[O:23])=[CH:18][CH:17]=2)=[C:9]([O:11][CH2:12][CH:13]=[CH2:14])[CH:10]=1)[CH:2]=[CH2:3].[H-].[Na+].[CH3:42]I.[Cl-].[NH4+]>CN(C)C=O>[CH2:1]([O:4][C:5]1[C:6]([CH2:38][CH3:39])=[C:7]([CH2:27][C:28]([N:30]([CH2:35][CH2:36][O:37][CH3:42])[CH2:31][CH2:32][O:33][CH3:34])=[O:29])[C:8]([C:15](=[O:26])[C:16]2[CH:17]=[CH:18][C:19]([S:22]([CH3:25])(=[O:23])=[O:24])=[CH:20][CH:21]=2)=[C:9]([O:11][CH2:12][CH:13]=[CH2:14])[CH:10]=1)[CH:2]=[CH2:3]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 23116349HCID 23116349, Verbindung

Produkt 1

HCID 23116231HCID 23116231, VerbindungAusbeute 21,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel

Versuchsvorschrift

(Step 1) 2-[3,5-Diallyloxy-2-ethyl-6-(4-methanesulfonylbenzoyl)phenyl]-N-(2-hydroxyethyl)-N-(2-methoxyethyl)acetamide (450 mg, 0.76 mmol) obtained in Example 96, Step 1 was dissolved in N,N-dimethylformamide (10 mL), and a 60% sodium hydride dispersion in mineral oil (50 mg, 1.3 mmol) was added thereto in an atmosphere of argon with stirring under ice-cooling. The reaction mixture was stirred at room temperature for 30 minutes, and methyl iodide (0.05 mL, 0.8 mmol) was added dropwise thereto, followed by further stirring for 12 hours. After the reaction mixture was ice-cooled, a saturated aqueous solution of ammonium chloride was added thereto to stop the reaction, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane=2/1) to obtain 2-[3,5-diallyloxy-2-ethyl-6-(4-methanesulfonylbenzoyl)phenyl]-N,N-bis(2-methoxyethyl)acetamide (95 mg, 21%).

Aufarbeitung

  1. temperaturecooling
  2. stirringThe reaction mixture was stirred at room temperature for 30 minutes
  3. stirringby further stirring for 12 hours
  4. temperaturecooled
  5. customthe reaction
  6. extractionfollowed by extraction with ethyl acetate
  7. washThe organic layer was washed with a saturated aqueous solution of sodium chloride
  8. dry with materialdried over anhydrous sodium sulfate
  9. concentrationconcentrated under reduced pressure
  10. customThe resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane=2/1)

Quellen und Nachweise

ORD-Eintrag
ord-2ac52ef7e0554e1cbb57d397a71407b9
Quelldatensatz
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07538224B2

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