HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373965Generated: October 30, 2026
Acetic Acid → 6-Butyl-4-methoxycarbonyl-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine
https://huagongshe.com/reaction/373965
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Butyl-5-(4-iodobenzyl)-2-methylpyrimidine-4-carbonitrile | HCID 19018800 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Butyl-4-methoxycarbonyl-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine | HCID 19018794 | 46% |
Reaction Steps
To a solution of 306 mg 6-butyl-4-cyano-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine in 6 mL methanol was added 0.885 mL (~7.81 mmol) 30% H2O2 and 0.937 mL (2.34 mmol) 2.5N NaOH. The mixture was allowed to stir for 1 hour at room temperature. To the mixture was added ~1 mL HOAc. Solvent was removed in vacuo. The crude material (409 mg) was dissolved in ~20 mL methanol. To this was added 4.0 g Amberlyst-15®. The mixture was heated to 60° for 18 hours. After cooling to room temperature, ~5 mL pyridine was added. After stirring for 1 hour, the mixture was filtered through powdered cellulose flock, stripped of solvent in vacuo, stripped from toluene to remove remaining pyridine, then was medium pressure chromatographed on silica gel using 25% EtOAc/hexane to give 152 mg of the title compound, 46% yield. R f 0.21 in 30% EtOAc/hexane, visualized by UV and ammonium molybdate/ceric sulfate stain; 1H-NMR (300 MHz, CDCl3); δ7.58 (m, 2H0, 6.81 (m, 2H), 4.12 (s, 2H), 3.87 (s, 3H), 2.75 (s, 3H), 2.67 (3 line m, 2H), 1.53 (m, 2H), 1.31 (m, 2H), 0.86 (3 line m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05166206 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-a11be5a0fa2449c2a5efc5fa5cd0a171 |
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| Source note | uspto-grants-1992_11 |
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