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Sodium hydride → HCID 68784837, Verbindung

HRID 2266525
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2266525
[H-].[Na+].[CH3:3][CH2:4][C:5](=[O:11])[CH2:6][C:7](=[O:10])[CH2:8][CH3:9].Br[CH2:13][C:14]1[CH:19]=[CH:18][C:17]([S:20]([CH3:23])(=[O:22])=[O:21])=[CH:16][CH:15]=1>CN(C)C=O.O>[CH3:23][S:20]([C:17]1[CH:18]=[CH:19][C:14]([CH2:13][CH:6]([C:5](=[O:11])[CH2:4][CH3:3])[C:7](=[O:10])[CH2:8][CH3:9])=[CH:15][CH:16]=1)(=[O:21])=[O:22]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 24758Sodium hydrideHCID 819233,5-HeptanedioneHCID 27335814-(Methylsulfonyl)benzyl Bromide

Produkt 1

HCID 68784837HCID 68784837, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 6228Dimethylformamide
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

Sodium hydride (60% in oil, 0.17 g) was added portionwise to a stirred solution of heptane-3,5-dione (0.54 mL) in N,N-dimethylformamide (4.0 mL) at 0-10° C. The resulting mixture was stirred at 0-10° C. for 10 minutes and then a solution of 1-bromomethyl-4-methanesulfonylbenzene (1.2 g) in N,N-dimethylformamide (2.0 mL) was added dropwise. The resulting mixture was stirred at room temperature for 18 hours, diluted with water and extracted with ethyl acetate. The combined extracts were washed with water and saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was removed under reduced pressure and purification of the residue by column chromatography on silica gel, eluting with a mixture of ethyl acetate and cyclohexane (1:4 by volume) gave title compound as a white solid, 0.61 g.

Aufarbeitung

  1. stirringThe resulting mixture was stirred at room temperature for 18 hours
  2. extractionextracted with ethyl acetate
  3. washThe combined extracts were washed with water and saturated aqueous sodium chloride solution
  4. dry with materialdried over magnesium sulfate
  5. customThe solvent was removed under reduced pressure and purification of the residue by column chromatography on silica gel
  6. washeluting with a mixture of ethyl acetate and cyclohexane (1:4 by volume)

Quellen und Nachweise

ORD-Eintrag
ord-e1ffe61854fc42ebbae98f6b66d8d7f7
Quelldatensatz
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07858640B2

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