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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443673Generated: October 25, 2026

Sodium hydride → 8-[4-(2-Isopropoxyphenyl)imidazol-1-yl]octanoic acid methyl ester

https://huagongshe.com/reaction/1443673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethyl 8-bromooctanoateHCID 11107373—
Reactant4-[2-(propan-2-yloxy)phenyl]-1H-imidazoleHCID 178458285—
CatalystTetrabutylammonium IodideHCID 67553—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product8-[4-(2-Isopropoxyphenyl)imidazol-1-yl]octanoic acid methyl esterHCID 5916780057.6%

Reaction Steps

Add sodium hydride (1.82 g, 38 mmol) to a suspension of 4-(2-isopropoxyphenyl)-1H-imidazole (5.01 g, 25 mmol) in THF (125 mL) at 0° C. under nitrogen, and warm the mixture to room temperature and stir for 1 hour. Cool the mixture to 0° C. and add 8-bromooctanoic acid methyl ester (5.98 g, 25 mmol) and tetra-n-butylammonium iodide (0.55 g, 1.5 mmol) and warm the mixture to room temperature to stir for 8 hours. Dilute the mixture with water (20 mL) and remove the solvent under reduced pressure. Dilute the residue with ethyl acetate (300 mL), wash with water (100 mL) and brine (100 mL), dry over sodium sulfate, and remove the solvent under reduced pressure to provide 8-[4(2-isopropoxyphenyl)imidazol-1-yl]octanoic acid methyl ester (5.16 g, 57%), which is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662771B2
Source datasetuspto-grants-2010_02
ORD IDord-5ff5dad245534f1998240ec632a649a2
Source noteuspto-grants-2010_02