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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465922Generated: October 30, 2026

Acetic Acid → HCID 178418660, compound

https://huagongshe.com/reaction/465922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1H-Imidazole-4-carbaldehydeHCID 76428—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 11240788HCID 11240788—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 178418660HCID 17841866090.7%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155101
Source datasetuspto-grants-1992_10
ORD IDord-43678e1aaa9a4d789e9c75f96d7c1c8c
Source noteuspto-grants-1992_10