Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373963Generated: October 30, 2026

Sodium Iodide → 6-Butyl-4-iodo-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine

https://huagongshe.com/reaction/373963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantHydrogen iodideHCID 24841—
Reactant6-Butyl-4-chloro-2-methyl-5-[(4-iodophenyl)methyl]pyrimidineHCID 19018795—
SolventAcetoneHCID 180—
Product6-Butyl-4-iodo-2-methyl-5-[(4-iodophenyl)methyl]pyrimidineHCID 1901879699.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 380 mg (0.947 mmol) 6-butyl-4-chloro-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine in 10 mL acetone were added 0.119 mL 57% HI (0.900 mmol) and 851 mg (5.68 mmol) NaI. The mixture was warmed to 40° C. for 2.5 hours. As the reaction proceeds, NaCl can be seen precipitating out of solution. The mixture was diluted with brine and saturated NaHCO3 solution. The mixture was extracted 3 times with ether. The combined organic material was dried over MgSO4 and decolorized with activated charcoal, was stripped of solvent in vacuo, then was medium pressure chromatographed on silica gel using 10% EtOAc/hexane to give 440 mg of 6-butyl-4-iodo-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine, 94% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166206
Source datasetuspto-grants-1992_11
ORD IDord-ba47aa0b4c304e65a3971af76ba70c68
Source noteuspto-grants-1992_11