HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254204Generated: October 25, 2026
Potassium Carbonate → 3-(4-Ethoxy-6-trifluoromethylpyrimidin-5-ylmethylthio)-5-chloromethyl-5-methyl-2-isoxazoline
https://huagongshe.com/reaction/254204
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Methylsulfonyl-5-chloromethyl-5-methyl-2-isoxazoline | HCID 11195206 | — |
| Reactant | Sodium hydrosulfide hydrate | HCID 16211346 | — |
| Reactant | 5-Bromomethyl-4-ethoxy-6-trifluoromethylpyrimidine | HCID 17862857 | — |
| Reactant | Sodium Formaldehyde Sulfoxylate | HCID 23689980 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(4-Ethoxy-6-trifluoromethylpyrimidin-5-ylmethylthio)-5-chloromethyl-5-methyl-2-isoxazoline | HCID 22934894 | 30.3% |
Reaction Steps
3.4 g (42.3 mmoles) of sodium hydrosulfide hydrate (purity: 70%) was added into a solution of 4.6 g (21.6 mmoles) of 3-methylsulfonyl-5-chloromethyl-5-methyl-2-isoxazoline dissolved in 70 ml of DMF. The mixture was stirred for 2 hours. Then, there were added 3.0 g (21.6 mmoles) of potassium carbonate, 3.3 g (21.6 mmoles) of Rongalit and 5-bromomethyl-4-ethoxy-6-trifluoromethylpyrimidine. The mixture was stirred at room temperature for 21 hours to give rise to a reaction. After the completion of the reaction, the reaction mixture was poured into water and extraction with ethyl acetate was conducted. The resulting organic layer was washed with an aqueous sodium chloride solution, followed by drying over anhydrous magnesium sulfate. The resulting solution was subjected to reduced pressure distillation to remove the solvent contained therein. The residue was purified by silica gel column chromatography (solvent system: hexane-ethyl acetate) to obtain 1.9 g (yield: 30.3%) of 3-(4-ethoxy-6-trifluoromethylpyrimidin-5-ylmethylthio)-5-chloromethyl-5-methyl-2-isoxazoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875606B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-9c5e06a7a55f4f6baaa213ad8b2a5e04 |
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| Source note | uspto-grants-2011_01 |
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