Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081872Generated: October 31, 2026

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

https://huagongshe.com/reaction/2081872

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-butyl-5-formyl-4-iodo-1H-imidazol-1-yl)methyl]naphthalene-1-carboxylateHCID 1993681185.2%

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 reaction mixture was poured into water and the resulting solid 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 numberUS05185351
Source datasetuspto-grants-1993_02
ORD IDord-ad302fa673694430be9f95b736cf1b84
Source noteuspto-grants-1993_02