Hydrochloric Acid → HCID 18354914, compound

HRID 1533790Notes

Reaction equation

HRID 1533790 reaction equation
[CH:1]([C:3]1[NH:7][C:6]2[CH:8]=[CH:9][CH:10]=[C:11]([C:12]([O:14][CH3:15])=[O:13])[C:5]=2[N:4]=1)=[O:2].CC(=CC)C.P([O-])(O)(O)=[O:22].[Na+].Cl([O-])=O.[Na+].Cl>O.C(O)(C)(C)C>[C:1]([C:3]1[NH:7][C:6]2[CH:8]=[CH:9][CH:10]=[C:11]([C:12]([O:14][CH3:15])=[O:13])[C:5]=2[N:4]=1)([OH:22])=[O:2]

Participants

8

Procedure

To a suspension of methyl 2-formyl-1H-benzimidazole-4-carboxylate (460 mg) in a mixture of water (3.2 ml) and t-butyl alcohol (12 ml) were added 2-methyl-2-butene (700 mg) and sodium dihydrogenphosphate (387 mg) in water bath. To the mixture was added portionwise sodium chlorite (901 mg) and stirred for 1 day at same temperature. The reaction mixture was cooled in an ice bath, adjusted to pH 4 with 1N hydrochloric acid and the precipitate was collected by vacuum filtration. The precipitate was washed with ethyl acetate and methanol to give methyl 2-carboxy-1H-benzimidazole-4-carboxylate (400 mg).

Workup

  1. temperatureThe reaction mixture was cooled in an ice bath
  2. filtrationthe precipitate was collected by vacuum filtration
  3. washThe precipitate was washed with ethyl acetate and methanol

Sources & evidence

ORD record
ord-29ca2b0fc1bb447c9ac19de4cdeec2e8
Source dataset
uspto-grants-2001_03
Patent number
US06207693B1

Reaction notes

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