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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616549Generated: October 29, 2026

Ammonium Acetate → 7-[5-(2-methoxyphenyl)-1H-imidazol-2-yl]heptanoic acid methyl ester

https://huagongshe.com/reaction/1616549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
Reactant7-[2-(2-Methoxyphenyl)-2-oxoethylcarbamoyl]heptanoic acid methyl esterHCID 68487925—
SolventAcetic AcidHCID 176—
Product7-[5-(2-methoxyphenyl)-1H-imidazol-2-yl]heptanoic acid methyl esterHCID 5916776144%

Reaction Steps

Heat a mixture of ammonium acetate (16.5 g, 214 mmol) and 7-[2-(2-methoxyphenyl)-2-oxoethylcarbamoyl]heptanoic acid methyl ester (14.2 g, 42.3 mmol) in acetic acid (300 mL) at reflux under nitrogen for 15 hours. Remove the solvent under reduced pressure. Dilute the residue in ethyl acetate (500 mL) and adjust to pH 8 with saturated aqueous sodium bicarbonate solution. Extract the aqueous layer with additional ethyl acetate (200 mL) and dry the combined organic extracts over sodium sulfate and remove the solvent under reduced pressure. Purify the residue by flash column chromatography on silica gel, eluting with ethyl acetate, to afford 7-[5-(2-methoxyphenyl)-1H-imidazol-2-yl]heptanoic acid methyl ester (5.86 g, 44%): APCI mass spectrum m/z 317 [C18H24N2O3+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765796B2
Source datasetuspto-grants-2014_07
ORD IDord-f5c51872cb424c24b380acc96e1ad7e9
Source noteuspto-grants-2014_07