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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | 6-Butyl-4-chloro-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine | HCID 19018795 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 6-Butyl-4-iodo-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine | HCID 19018796 | 99.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05166206 |
|---|
| Source dataset | uspto-grants-1992_11 |
|---|
| ORD ID | ord-ba47aa0b4c304e65a3971af76ba70c68 |
|---|
| Source note | uspto-grants-1992_11 |
|---|