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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433630Generated: October 30, 2026

Acetic Acid → [1-(3-Bromo-5-fluoro-phenyl)-1H-imidazol-4-yl]-methanol

https://huagongshe.com/reaction/433630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl orthoformateHCID 31214—
ReactantEthyl nitroacetateHCID 69379—
Reactant3-Bromo-5-fluoroanilineHCID 15020155—
CatalystIronHCID 23925—
Product[1-(3-Bromo-5-fluoro-phenyl)-1H-imidazol-4-yl]-methanolHCID 23445045—

Reaction Steps

Following the general method described in example 293, 3-bromo-5-fluoroaniline (K. Yoshiizumi et al., Bioorg.Med.Chem.Lett., 1998, 8, 3397-3402) was reacted with triethyl orthoformate, ethyl nitroacetate and acetic acid followed by treatment with triethyl orthoformate, iron and acetic acid and subsequent alkaline hydrolysis. The isolated acid was directly reduced according to example 264, by reaction with BH3 THF complex followed by hydrolytic workup and the title compound was obtained as a light brown solid. Mp. 134-138° C. (AcOEt/hexane), MS: m/e=271 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06667335B2
Source datasetuspto-grants-2003_12
ORD IDord-41dd5ccc12cd4130bc2fb39a9b71f586
Source noteuspto-grants-2003_12