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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110055Generated: November 1, 2026

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

https://huagongshe.com/reaction/1110055

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 19018796947%

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, 947% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324729
Source datasetuspto-grants-1994_06
ORD IDord-5fda26c064e04921ad2a832dfd2b4dc2
Source noteuspto-grants-1994_06