Acetic Acid → 1,2-dimethyl-4-methoxy-1H-benzimidazole

HRID 2287540Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2287540
[NH2:1][C:2]1[C:9]([O:10][CH3:11])=[CH:8][CH:7]=[CH:6][C:3]=1[NH:4][CH3:5].[C:12](O)(=O)[CH3:13]>Cl>[CH3:5][N:4]1[C:3]2[CH:6]=[CH:7][CH:8]=[C:9]([O:10][CH3:11])[C:2]=2[N:1]=[C:12]1[CH3:13]

Komponenten

4

Edukt 2

HCID 176Acetic AcidHCID 106069363-methoxy-N1-methylbenzene-1,2-diamine

Produkt 1

HCID 107024241,2-dimethyl-4-methoxy-1H-benzimidazoleAusbeute 87,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 313Hydrochloric AcidLösungsmittel

Versuchsvorschrift

A suspension of 2-amino-3-methoxy-N-methylaniline (671 mg) and acetic acid (265 mg) in 4N hydrochloric acid (3.5 ml) was refluxed for 10 hours. Insoluble material was filtered off, and the filtrate was adjusted to pH 7 with saturated sodium bicarbonate solution, and extracted with dichloromethane. The organic layers were combined, washed with brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by silica gel flash chromatography (dichloromethane:methanol=40:1, v/v) to give 1,2-dimethyl-4-methoxy-1H-benzimidazole (680 mg).

Aufarbeitung

  1. temperaturewas refluxed for 10 hours
  2. filtrationInsoluble material was filtered off
  3. extractionextracted with dichloromethane
  4. washwashed with brine
  5. dry with materialdried over magnesium sulfate
  6. customevaporated in vacuo
  7. customThe residue was purified by silica gel flash chromatography (dichloromethane

Quellen und Nachweise

ORD-Eintrag
ord-78c40a1594544a43b12d08dba3f3a2ec
Quelldatensatz
uspto-grants-2000_07
Patentnummer
US06083961

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