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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37219Generated: October 29, 2026

Sodium hydride → tert-Butyl 2-[4-(2-butyl-4-chloro-5-formyl-imidazol-1-yl-methyl)phenyl]-2-cyclopentylacetate

https://huagongshe.com/reaction/37219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 2-(4-(bromomethyl)phenyl)-2-cyclopentylacetateHCID 15225592—
ReactantHCID 178418251HCID 178418251—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 2-[4-(2-butyl-4-chloro-5-formyl-imidazol-1-yl-methyl)phenyl]-2-cyclopentylacetateHCID 15225591—

Reaction Conditions

Temperature0 °C

Reaction Steps

1.6 g (0.053 mol) of sodium hydride (80%) are suspended under protective gas in 50 ml of DMF, 10 g (0.053 mol) of 2-butyl-5-formyl-4-chloroimidazole (preparation as described in EP 324,377) in 100 ml of DMF are added dropwise at 0° C., the mixture is subsequently stirred for 15 minutes at 0° C., and 18.9 g (0.053 mol) of tert-butyl 2-(4-bromomethylphenyl)-2-cyclopentyl-acetate in 100 ml of DMF are added dropwise. Stirring is continued for 2 hours at 0° C., the solvent is evaporated, the residue is taken up in diethyl ether, the mixture is filtered, and the product is concentrated and then chromatographed over silica gel 60 using dichloromethane. Yield: 16.2 g (66.7% of theory)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420149
Source datasetuspto-grants-1995_05
ORD IDord-bbf55e86722a4393af6e6479b9f83698
Source noteuspto-grants-1995_05