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Ammonium Chloride → 2-(1,3-Isoindolinedion-2-yl)-5-(2,2-dimethyl-3-methoxycarbonyl-propionyl)indane

HRID 1598561
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1598561
C[Si]([N-][Si](C)(C)C)(C)C.[Li+].C([Li])CCC.[C:16]1(=[O:40])[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[C:18](=[O:25])[N:17]1[CH:26]1[CH2:34][C:33]2[C:28](=[CH:29][CH:30]=[C:31]([C:35](=[O:39])[CH:36]([CH3:38])[CH3:37])[CH:32]=2)[CH2:27]1.Br[CH2:42][C:43]([O:45][CH3:46])=[O:44].[Cl-].[NH4+]>O1CCCC1>[C:16]1(=[O:40])[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[C:18](=[O:25])[N:17]1[CH:26]1[CH2:34][C:33]2[C:28](=[CH:29][CH:30]=[C:31]([C:35](=[O:39])[C:36]([CH3:37])([CH3:38])[CH2:42][C:43]([O:45][CH3:46])=[O:44])[CH:32]=2)[CH2:27]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 25517Ammonium ChlorideHCID 60984Methyl bromoacetateHCID 2733832Lithium hexamethyldisilazaneHCID 189297332-(1,3-Isoindolinedion-2-yl)-5-(2-methylpropionyl)indaneHCID 178418339Butyllithium

Produkt 1

HCID 18929738
2-(1,3-Isoindolinedion-2-yl)-5-(2,2-dimethyl-3-methoxycarbonyl-propionyl)indane
Ausbeute 51,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel3×

Reaktionsbedingungen

Temperatur
-40 °C

Versuchsvorschrift

Lithium bis(trimethylsilyl)amide prepared from 1.78 g of 1,1,1,3,3,3-hexamethylsilazane and n-butyl lithium (6.9 ml of 1.6M hexane solution), dissolved in 50 ml of tetrahydrofuran was cooled to -40° C., and 3.30 g of 2-(1,3-isoindolinedion-2-yl)-5-(2-methylpropionyl)indane dissolved in 50 ml of tetrahydrofuran was added dropwise thereto over 15 minutes. The mixture was stirred at 0° C. for 20 minutes and cooled to -30° C. To the mixture was added dropwise 1.68 g of methyl bromoacetate dissolved in 10 ml of tetrahydrofuran, and the mixture was stirred at room temperature for 2.5 hours. To the reaction mixture was added a saturated ammonium chloride solution, the mixture was extracted with ethyl acetate, the extract was dried, and then the solvent was removed. The residue was purified by silica gel column chromatography (eluted by n-hexane:ethyl acetate =4:1). The resulting crystals were recrystallized from ethyl acetate-n-hexane to obtain 2.06 g of 2-(1,3-isoindolinedion-2-yl)-5-(2,2-dimethyl-3-methoxycarbonyl-propionyl)indane.

Aufarbeitung

  1. additionwas added dropwise
  2. temperaturecooled to -30° C
  3. stirringthe mixture was stirred at room temperature for 2.5 hours
  4. extractionthe mixture was extracted with ethyl acetate
  5. customthe extract was dried
  6. customthe solvent was removed
  7. customThe residue was purified by silica gel column chromatography (eluted by n-hexane:ethyl acetate =4:1)
  8. customThe resulting crystals were recrystallized from ethyl acetate-n-hexane

Quellen und Nachweise

ORD-Eintrag
ord-ddde2845c71f418cb8bc8fc2ed367554
Quelldatensatz
uspto-grants-1998_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05739132

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