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Hydrochloric Acid → 2,3-Dimethoxy-benzamidine

HRID 1008232
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1008232
C[Si](C)(C)[NH:3][Si](C)(C)C.C([Li])CCC.[CH3:15][O:16][C:17]1[C:24]([O:25][CH3:26])=[CH:23][CH:22]=[CH:21][C:18]=1[C:19]#[N:20].Cl>CCOCC.CCCCCC>[CH3:15][O:16][C:17]1[C:24]([O:25][CH3:26])=[CH:23][CH:22]=[CH:21][C:18]=1[C:19]([NH2:3])=[NH:20]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 13838HexamethyldisilazaneHCID 218622,3-DimethoxybenzonitrileHCID 178418339Butyllithium

Produkt 1

HCID 37009942,3-Dimethoxy-benzamidine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 3283Diethyl EtherLösungsmittel
HCID 8058HexaneLösungsmittel

Versuchsvorschrift

To a solution of 20 g 1,1,1,3,3,3-hexamethyldisilazane in 150 mL dry ether was added 5 mL 2.4 M n-butyllithium in hexane. After 10 min at room temperature, 16.3 g 2,3-dimethoxybenzonitrile was added in one portion and the mixture was kept at room temperature for 16 h. The reaction mixture was then poured onto excess 3N HCl. The aqueous layer was separated, basified with 50% NaOH and the product was extracted three times with 10% methanol in methylene chloride. The combined organic extracts were dried over potassium carbonate and the solvents removed in vacuo to afford 2,3-dimethoxybenzamidine as a glassy solid.

Aufarbeitung

  1. waitthe mixture was kept at room temperature for 16 h
  2. customThe aqueous layer was separated
  3. extractionthe product was extracted three times with 10% methanol in methylene chloride
  4. dry with materialThe combined organic extracts were dried over potassium carbonate
  5. customthe solvents removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-d9e1253c4d874c118f2481b726c917c3
Quelldatensatz
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06797824B2

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