Acetic Acid → HCID 178418660, compound

HRID 2210787Notes

Reaction equation

HRID 2210787 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1/[CH:8]=[CH:9]/[C:10]([O:12][CH3:13])=[O:11].[CH:14]([C:16]1[N:17]=[CH:18][NH:19][CH:20]=1)=O.[BH4-].[Na+].C(O)(=O)C>CO.C(Cl)(Cl)Cl>[NH:19]1[CH:20]=[C:16]([CH2:14][NH:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2/[CH:8]=[CH:9]/[C:10]([O:12][CH3:13])=[O:11])[N:17]=[CH:18]1

Participants

7

Reactant 4

HCID 176Acetic AcidHCID 764281H-Imidazole-4-carbaldehydeHCID 4311764Sodium borohydride3×HCID 11240788HCID 11240788, compound

Product 1

HCID 178418660HCID 178418660, compoundYield 90.7%

Reagents, catalysts & solvents 2

HCID 887MethanolSolvent2×HCID 6212ChloroformSolvent

Procedure

A solution of methyl (E)-3-(2-aminophenyl)propenoate (531.6 mg) and 4-formylimidazole (317.1 mg) in methanol (7.0 ml) was stirred at ambient temperature for 18 hours. To the reaction mixture was added sodium borohydride (56.5 mg) under stirring and cooling in an ice-bath. After the mixture was stirred for 2 hours at ambient temperature, sodium borohydride (56.5 mg) was added thereto. The mixture was stirred for 2 hours at ambient temperature. To the reaction mixture was added acetic acid in order to decompose the excess sodium borohydride and the methanol was removed under reduced pressure. To the residue were added diluted hydrochloric acid and ethyl acetate under stirring. The separated aqueous layer was basified with aqueous sodium bicarbonate and extracted twice with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and evaporated to give a residue, which was subjected to column chromatography on silica gel with an eluent of a mixture of chloroform and methanol (20:1) to afford pure methyl (E)-3-[2-(4-imidazolylmethylamino)phenyl]-propenoate (0.7 g) as an oil.

Workup

  1. temperaturecooling in an ice-bath
  2. stirringAfter the mixture was stirred for 2 hours at ambient temperature
  3. stirringThe mixture was stirred for 2 hours at ambient temperature
  4. customthe methanol was removed under reduced pressure
  5. additionTo the residue were added diluted hydrochloric acid and ethyl acetate
  6. stirringunder stirring
  7. extractionextracted twice with ethyl acetate
  8. washThe extract was washed with water
  9. dry with materialdried over magnesium sulfate
  10. customevaporated
  11. customto give a residue, which

Sources & evidence

ORD record
ord-7bd097833c1e47a4b6d19b70e24b0580
Source dataset
uspto-grants-1995_10
Patent number
US05461048

Reaction notes

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