HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455003Generated: October 31, 2026
Sodium Hydroxide → 2-[[(2,3-Difluorophenyl)methyl]thio]-4,6(1H,5H)-pyrimidinedione
https://huagongshe.com/reaction/1455003
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(Bromomethyl)-2,3-difluoro-benzene | HCID 517984 | — |
| Reactant | Thiobarbituric acid | HCID 2723628 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 2-[[(2,3-Difluorophenyl)methyl]thio]-4,6(1H,5H)-pyrimidinedione | HCID 68905089 | — |
Reaction Steps
Sodium hydroxide (6.1 g) in ethanol (20 ml) and water (20 ml) was added to a suspension of 4,6-dihydroxy-2-thiopyrimidine in ethanol/water (120 ml/120 ml). 2,3-difluorobenzyl bromide (28.4 g) was added dropwise to this solution. The mixture was heated at 60° C. for 2 h and stirred at room temperature for 20 h. The solids were filtered and washed with water (200 ml), isopropanol (20 ml) and dried in vacuo at 40° C. for 24 h to yield the subtitle compound. Yield 31.0 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07482355B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-58e8a820cad24e128ef47ef078896cfa |
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| Source note | uspto-grants-2009_01 |
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