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Hydrochloric Acid → 1H-Benzimidazole-1-butanamine

HRID 1902452
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1902452
[N:1]1([CH2:10][CH2:11][CH2:12][C:13]#[N:14])[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1.Cl>[Pd].C(O)C>[N:1]1([CH2:10][CH2:11][CH2:12][CH2:13][NH2:14])[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 313Hydrochloric AcidHCID 130667534-(1H-Benzimidazol-1-yl)butanenitrile

Produkt 1

HCID 43794811H-Benzimidazole-1-butanamine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysatorHCID 702EthanolLösungsmittel

Versuchsvorschrift

A solution was prepared from 8.9 grams of the nitrile and 150 ml of absolute ethanol, 0.8 grams of palladium on charcoal and 8 ml of concentrated hydrochloric acid were added, and the resulting mixture was hydrogenated at room temperature and pressure for 48 hours. The reaction mixture was then filtered, the solvent was evaporated from the filtrate, and the residue was treated with aqueous 2 N sodium hydroxide solution and extracted with chloroform. The chloroform solution was dried and then distilled to give 1H-benzimidazole-1-butanamine boiling at about 180°-186° C. at 1.2 mm pressure.

Aufarbeitung

  1. additionwere added
  2. customwas hydrogenated at room temperature
  3. filtrationThe reaction mixture was then filtered
  4. customthe solvent was evaporated from the filtrate
  5. additionthe residue was treated with aqueous 2 N sodium hydroxide solution
  6. extractionextracted with chloroform
  7. dry with materialThe chloroform solution was dried
  8. distillationdistilled

Quellen und Nachweise

ORD-Eintrag
ord-b654d2e2c722415bb862048485a040e4
Quelldatensatz
uspto-grants-1982_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04363808

Notizen zur Reaktion

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