HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844860Generated: October 30, 2026
Water → 5-Iodo-1,3-diethyl-6-methyl uracil
https://huagongshe.com/reaction/844860
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Iodo-6-methyluracil | HCID 319986 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Iodo-1,3-diethyl-6-methyl uracil | HCID 22613712 | 60% |
Reaction Steps
To a suspension of 5-iodo-6-methyl uracil (20.97 mmol, 5.45 g) and powdered potassium carbonate (60 mmol, 8.29 g) in DMF (188 mL) was added ethyl iodide (83.88 mmol, 6.7 mL). The reaction mixture was stirred for 15 h at room temperature and was poured into water (150 mL) and ethyl acetate (150 mL). The layers were separated and the aqueous layer was extracted with ethyl acetate (2×100 mL). The combined extracts were washed with brine solution (150 mL) and were dried over anhydrous magnesium sulfate. Filtration of the drying agent and concentration gave a crude solid which was triturated with dichloromethane/diethyl ether/hexanes (1:1:1) to afford 3.89 g (60% yield) of 5-iodo-1,3-diethyl-6-methyl uracil as a white crystalline solid: mp 159-161.5° C. EI-HRMS m/e calcd for C9H13IN2O2 (M+) 308.0022, found 308.0018.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06380387B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-fa7a37135efa4b3fa09b279c5326e2af |
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| Source note | uspto-grants-2002_04 |
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