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Acetic Acid → Racemic 3-[5-(tert-butyl-dimethyl-silanyloxy)-3,3-dim ethyl-1-nitromethyl-pentyl]-6-chloro-1,3-dihydro-indol-2-one

HRID 2065416
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2065416
[N+:1]([CH3:4])([O-:3])=[O:2].C[O-].[Na+].[C:8]([Si:12]([CH3:33])([CH3:32])[O:13][CH2:14][CH2:15][C:16]([CH3:31])([CH3:30])[CH2:17]/[CH:18]=[C:19]1\[C:20](=[O:29])[NH:21][C:22]2[C:27]\1=[CH:26][CH:25]=[C:24]([Cl:28])[CH:23]=2)([CH3:11])([CH3:10])[CH3:9].C(O)(=O)C>CO>[C:8]([Si:12]([CH3:32])([CH3:33])[O:13][CH2:14][CH2:15][C:16]([CH3:31])([CH3:30])[CH2:17][CH:18]([CH:19]1[C:27]2[C:22](=[CH:23][C:24]([Cl:28])=[CH:25][CH:26]=2)[NH:21][C:20]1=[O:29])[CH2:4][N+:1]([O-:3])=[O:2])([CH3:10])([CH3:9])[CH3:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 176Acetic AcidHCID 6375NitromethaneHCID 10942334Sodium MethoxideHCID 86656671Z-3-[5-(tert-butyl-dimethyl-silanyloxy)-3,3-dimethyl-pentylidene]-6-chloro-1,3-dihydro-indol-2-one

Produkt 1

HCID 58399000Racemic 3-[5-(tert-butyl-dimethyl-silanyloxy)-3,3-dim ethyl-1-nitromethyl-pentyl]-6-chloro-1,3-dihydro-indol-2-one
Ausbeute 64,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel2×

Versuchsvorschrift

To a solution of nitromethane (Aldrich) (0.21 g, 3.5 mmol) in methanol (20 mL) was slowly added a methanolic solution (Aldrich, 25 wt. %) of sodium methoxide (0.74 g, 3.5 mmol). After the mixture was stirred at room temperature for 10 min, a solution of E/Z-3-[5-(tert-butyl-dimethyl-silanyloxy)-3,3-dimethyl-pentylidene]-6-chloro-1,3-dihydro-indol-2-one (0.68 g, 1.7 mmol) in methanol (10 mL) was added. The reaction mixture was stirred at room temperature for 2 h, then acetic acid (0.6 g, 10 mmol) was added. The mixture was concentrated to a small volume, then the residue was partitioned between ethyl acetate and water. The organic layer was separated, the aqueous layer was extracted with ethyl acetate. The organic layers were combined, washed with saturated aqueous NaHCO3, brine, dried over MgSO4, and concentrated. The residue was purified by chromatography (EtOAc:hexanes=1:10) to give the racemic 3-[5-(tert-butyl-dimethyl-silanyloxy)-3,3-dim ethyl-1-nitromethyl-pentyl]-6-chloro-1,3-dihydro-indol-2-one as a white foam (0.5 g, 64%).

Aufarbeitung

  1. stirringThe reaction mixture was stirred at room temperature for 2 h
  2. concentrationThe mixture was concentrated to a small volume
  3. customthe residue was partitioned between ethyl acetate and water
  4. customThe organic layer was separated
  5. extractionthe aqueous layer was extracted with ethyl acetate
  6. washwashed with saturated aqueous NaHCO3, brine
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated
  9. customThe residue was purified by chromatography (EtOAc:hexanes=1:10)

Quellen und Nachweise

ORD-Eintrag
ord-9a32f88cbd5842e79ea190bbd29b9c60
Quelldatensatz
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08288431B2

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