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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707265Generated: October 30, 2026

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

https://huagongshe.com/reaction/1707265

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

Under protective gas, 1.6 g (0.053 mol) of sodium hydride (80% strength) are suspended in 50 ml of DMF, 10 g (0.053 mol) of 2-butyl-5-formyl-4-chloroimidazole (preparation according to EP 324,377) in 100 ml of DMF are added dropwise at 0° C., then the mixture is stirred at 0° C. for 15 min and 18.9 g (0.053 mol) of tertbutyl 2-(4-bromomethylphenyl)-2-cyclopentylacetate in 100 ml of DMF are added dropwise. The mixture is stirred for 2 h at 0° C., the solvent is evaporated, the residue is taken up in diethyl ether, the solid is filtered off and, after concentration, the residue is chromatographed on silica gel 60 using dichloromethane. Yield: 16.2 g (66.7% of theory) Solidification point: 101°-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05352687
Source datasetuspto-grants-1994_10
ORD IDord-907665d0913a41478a190a063a59651c
Source noteuspto-grants-1994_10