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O-Phenylenediamine → 2-Benzimidazolepropanol

HRID 1016430
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1016430
[C:1]1([NH2:8])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[NH2:7].[O:9]1[CH2:13][CH2:12][CH2:11][C:10]1=O>Cl>[NH:7]1[C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][C:1]=2[N:8]=[C:13]1[CH2:12][CH2:11][CH2:10][OH:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 7243O-PhenylenediamineHCID 7302Gamma-Butyrolactone

Produkt 1

HCID 754702-BenzimidazolepropanolAusbeute 95,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 313Hydrochloric AcidLösungsmittel

Versuchsvorschrift

A mixture of 5.4 g of 1,2-phenylenediamine and 4.5 g of dihydro-furan-2-one in 50 mL of 4N hydrochloric acid was heated to reflux for 20 h, 1 teaspoon of decolorizing carbon added, and after another 15 min reflux, filtered hot. The filtrate was concentrated under reduced pressure to near dryness, the residue made basic (pH=8) with saturated sodium bicarbonate and extracted into 3×80 mL of ether. The combined extracts were dried over magnesium sulfate and concentrated under reduced pressure. After drying under vacuum, 8.4 g of 3-(1H-benzimidazol-2-yl)-propan-1-ol was obtained as a solid.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureto reflux for 20 h
  3. addition1 teaspoon of decolorizing carbon added
  4. temperatureafter another 15 min reflux
  5. filtrationfiltered hot
  6. concentrationThe filtrate was concentrated under reduced pressure
  7. extractionextracted into 3×80 mL of ether
  8. dry with materialThe combined extracts were dried over magnesium sulfate
  9. concentrationconcentrated under reduced pressure
  10. customAfter drying under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-ed5d5172cefb464682d4c7af07dff6a6
Quelldatensatz
uspto-grants-2002_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06476041B1

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