Ammonia → 1H-benzimidazole-2-carbonitrile

HRID 1033222

Reaktionsgleichung

Reaktionsgleichung von HRID 1033222
Cl[C:2](Cl)(Cl)[C:3]1[NH:4][C:5]2[CH:11]=[CH:10][CH:9]=[CH:8][C:6]=2[N:7]=1.[NH3:14]>C(O)C>[C:2]([C:3]1[NH:4][C:5]2[CH:11]=[CH:10][CH:9]=[CH:8][C:6]=2[N:7]=1)#[N:14]

Komponenten

4

Versuchsvorschrift

5.3 Grams of 2-(trichloromethyl)benzimidazole compound [compound (104)] of the formula (XI) in which X is H and Z is OCF2O was suspended in 100 ml of ethanol. The resulting solution was added by drops to 40 ml of a 25% aqueous ammonia at 5° C. After stirring for 1 hour at 5° C. to room temperature, the reaction solution was poured into an ice/conc. hydrochloric acid mixture and extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous sodium sulfate. Removing the solvent from the dried layer by distillation gave 4.0 g of a 2-cyanobenzimidazole compound [compound (iv)] of the formula (II) in which X is H and Z is OCF2O.

Aufarbeitung

  1. extractionhydrochloric acid mixture and extracted with ethyl acetate
  2. washThe organic layer was washed with water
  3. dry with materialdried over anhydrous sodium sulfate
  4. customRemoving the solvent from the dried layer
  5. distillationby distillation

Quellen und Nachweise

ORD-Eintrag
ord-c2c55a029aa84f47aee5eac07f8ae2a0
Quelldatensatz
uspto-grants-1994_05
Patentnummer
US05310747

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