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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 342687생성일: 2026년 10월 26일

Tetrahydrofuran → 1-(2-Methylthiopyrimidin-4-yl)-2-(3-trifluoromethylphenyl)ethane-1,2-dione-1-oxime

https://huagongshe.com/reaction/342687

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Sodium HydroxideHCID 14798—
반응물2-[2-(Methylthio)pyrimidin-4-yl]-1-[3-(trifluoromethyl)phenyl]ethanoneHCID 10757458—
반응물Sodium NitriteHCID 23668193—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물1-(2-Methylthiopyrimidin-4-yl)-2-(3-trifluoromethylphenyl)ethane-1,2-dione-1-oximeHCID 136365326—

반응 단계

To a mixture of 2-(2-methylthiopyrimidin-4-yl)-1-(3-trifluoromethylphenyl)ethanone (4.5 g, 0.0144 mole) in acetic acid (67 mL), was added THF (54 mL) and water (9 mL). The mixture was cooled to +5° C. and a solution of sodium nitrite (1.34 g, 0.0194 mole) added dropwise while maintaining the temperature below +10° C. Upon completion of addition, the reaction was allowed to warm to room temperature for 1 hour, diluted with water (200 mL) and ethyl acetate (200 mL) and the pH adjusted to 7.5 with 3N NaOH. The layers were separated and the aqueous layer washed with ethyl acetate (100 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated to an oil. Yield 4.9 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05859041
출처 데이터셋uspto-grants-1999_01
ORD IDord-29bb2f0d30554742bb809c953a2bc56e
출처 메모uspto-grants-1999_01