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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 254204생성일: 2026년 10월 26일

Potassium Carbonate → 3-(4-Ethoxy-6-trifluoromethylpyrimidin-5-ylmethylthio)-5-chloromethyl-5-methyl-2-isoxazoline

https://huagongshe.com/reaction/254204

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3-Methylsulfonyl-5-chloromethyl-5-methyl-2-isoxazolineHCID 11195206—
반응물Sodium hydrosulfide hydrateHCID 16211346—
반응물5-Bromomethyl-4-ethoxy-6-trifluoromethylpyrimidineHCID 17862857—
반응물Sodium Formaldehyde SulfoxylateHCID 23689980—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물3-(4-Ethoxy-6-trifluoromethylpyrimidin-5-ylmethylthio)-5-chloromethyl-5-methyl-2-isoxazolineHCID 2293489430.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07875606B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-9c5e06a7a55f4f6baaa213ad8b2a5e04
출처 메모uspto-grants-2011_01