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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2347Generated: October 26, 2026

Water → Methyl 4-[(2-n-Butyl-5-formyl-4-iodo-1H-imidazol-5-yl)methyl]-1-naphthalene carboxylate

https://huagongshe.com/reaction/2347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Naphthalenecarboxylic acid, 4-(bromomethyl)-, methyl esterHCID 10333813—
Reactant2-Butyl-5-formyl-4-iodo-imidazoleHCID 178418262—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-[(2-n-Butyl-5-formyl-4-iodo-1H-imidazol-5-yl)methyl]-1-naphthalene carboxylateHCID 8675228885%

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of 29.53 g (0.214 mol) of powdered potassium carbonate, 60.00 g (0.214 mol) of 2-butyl-4-iodoimidazole-5-carboxaldehyde, and 65.68 g (0.235 mol) of methyl 4-bromomethylnaphthalene-1-carboxylate (E. A. Dixon, A. Fischer, and F. P. Robinson, Can. J. Chem. 59, 2629 (1981)) in 600 ml of dimethylformamide was stirred for 5 hours under argon at 70° C. An additional 6.56 g (0.0235 mol) of the bromomethyl ester was added and the suspension was stirred an additional 15 hours at 70° C. The mixture was poured into water and the solid which separated was collected by filtration, washed with water, and triturated several times with 250 ml of boiling methanol to give 86.8 g (85%) of a solid; mp 177.5°-179° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728842
Source datasetuspto-grants-1998_03
ORD IDord-ff9fddba17f84a17b2c77c4ed15d72d3
Source noteuspto-grants-1998_03