Citric Acid → (1,2-Dimethyl-1H-benzo[d]imidazol-5-yl)methanol

HRID 928447Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 928447
[CH3:1][N:2]1[C:6]2[CH:7]=[CH:8][C:9]([C:11](OC)=[O:12])=[CH:10][C:5]=2[N:4]=[C:3]1[CH3:15].O.O.O.O.O.O.O.O.O.O.S([O-])([O-])(=O)=O.[Na+].[Na+].C(O)(=O)CC(CC(O)=O)(C(O)=O)O.CC(=O)OCC>C1COCC1>[CH3:1][N:2]1[C:6]2[CH:7]=[CH:8][C:9]([CH2:11][OH:12])=[CH:10][C:5]=2[N:4]=[C:3]1[CH3:15]

Komponenten

6

Versuchsvorschrift

To a solution of Methyl 1,2-dimethyl-1H-benzo[d]imidazole-5-carboxylate (500 mg, 2.448 mmol) in THF (24.5 ml) Lithiumaluminium hydride (1 M in THF, 2.44 ml) was added at 0° C. After 2 hours sodium sulfate decahydrate and citric acid was added to the reaction to destroy the excess of lithiumaluminiumhydride. After 1 hour, methanol (25 ml) was added and the fine suspension was filtered off. The filtrate was evaporated under reduced pressure to afford a brown solid. EA (50 ml) was added and the suspension was treated in an ultra sonic bath. The solid was filtered off and this procedure was repeated twice. The yellow filtrate was evaporated under reduced pressure to afford crude (1,2-Dimethyl-1H-benzo[d]imidazol-5-yl)methanol.

Aufarbeitung

  1. customto destroy the excess of lithiumaluminiumhydride
  2. additionmethanol (25 ml) was added
  3. filtrationthe fine suspension was filtered off
  4. customThe filtrate was evaporated under reduced pressure
  5. customto afford a brown solid
  6. additionthe suspension was treated in an ultra sonic bath
  7. filtrationThe solid was filtered off
  8. customThe yellow filtrate was evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-7018b9a92df343af9db66a8f7dd2e912
Quelldatensatz
uspto-grants-2016_03
Patentnummer
US09290485B2

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