Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610950Generated: November 1, 2026

Water → HCID 22259354, compound

https://huagongshe.com/reaction/1610950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1H-imidazole-2-carbaldehydeHCID 24955—
ReactantHCID 12992838HCID 12992838—
SolventDimethylformamideHCID 6228—
ProductHCID 22259354HCID 22259354—

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of 1-tert-butoxy-4-(4-iodobutyl)benzene (10.0 g), 2-formyl-1H-imidazole (3.47 g) and potassium carbonate (4.16 g) in DMF (100 ml) was stirred at 70° C. for 17 hr. The reaction mixture was combined with water and extracted with ethyl acetate. The extract was successively washed with water (3 times) and saturated brine, dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give crude 1-[4-(4-tert-butoxyphenyl)butyl]-1H-imidazole-2-carbaldehyde as a pale brown oil. Sodium borohydride (1.25 g) was added to a solution of the compound in methanol (200 ml) at 0° C., and the mixture was stirred at 0° C. for 1 hr. The reaction mixture was combined with water, concentrated and extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (Chromatorex, 100-200 mesh, Fuji silicia chemical) (eluent; hexane:ethyl acetate=1:3 to ethyl acetate) to give the titled compound (8.29 g) as a colorless amorphous form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984653B2
Source datasetuspto-grants-2006_01
ORD IDord-6d77a9fcb7104f10aa331d0ee5d1699b
Source noteuspto-grants-2006_01