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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 883024생성일: 2026년 10월 26일

Methyl triflate → HCID 178448620, 화합물

https://huagongshe.com/reaction/883024

반응식

참여 물질

역할이름HCID투입량
반응물Methyl triflateHCID 9526—
반응물Ammonium HydroxideHCID 14923—
반응물n-(1-Butyl-3-tert-butyl-1h-pyrazol-5-yl)-2-fluoro-5-(trifluoromethyl)benzamideHCID 66643255—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물HCID 178448620HCID 17844862089.2%

반응 조건

온도100 °C

반응 단계

To a solution of Example 4B (50.2 g, 130 mmol) in toluene (500 mL) was added methyl trifluoromethanesulfonate (21.4 mL, 195 mmol). The mixture was warmed to 100° C. and stirred for 20 hours. The mixture was cooled to ambient temperature then diluted with water (200 mL) and acetone (500 mL). This solution was stirred for 30 minutes then concentrated NH4OH (100 mL) was added. The mixture was stirred for 30 minutes then partially concentrated under reduced pressure. The residue was diluted with EtOAc (300 mL) and brine (100 mL), the layers were separated and the aqueous phase was extracted with EtOAc (3×30 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography (SiO2, 80% hexanes/EtOAc to 100% EtOAc to 10% MeOH in EtOAc) and the fractions collected and concentrated. The material was then dissolved in EtOAc (150 mL) and was washed with 10% NaOH (100 mL). The layers were separated, the aqueous phase was extracted with EtOAc (3×50 mL) and the combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to give (46.3 g, 116 mmol, 89% yield) the title compound. MS (ESI+) m/z 400 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08236822B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-bf160eab9f8840e09caa881af15bf39b
출처 메모uspto-grants-2012_08