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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217871생성일: 2026년 10월 25일

1-Methylpyrrolidine → Prop-1-en-2-yl 5-(trifluoromethyl)pyridin-3-ylcarbamate

https://huagongshe.com/reaction/217871

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylpyrrolidineHCID 8454—
반응물Ethyl AcetateHCID 8857—
반응물Isopropenyl chloroformateHCID 93846—
반응물5-(Trifluoromethyl)pyridin-3-amineHCID 14051936—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물Prop-1-en-2-yl 5-(trifluoromethyl)pyridin-3-ylcarbamateHCID 59588859—

반응 조건

온도0 °C

반응 단계

5-(trifluoromethyl)pyridin-3-amine (883 mg, 5.45 mmol) was suspended in dry THF (20 mL) and N-methylpyrrolidine (680 μL, 6.54 mmol) was added to give a brown suspension. The mixture was cooled to 0° C. and isopropenyl chloroformate (715 μL, 6.54 mmol) was added dropwise over 15 min. The suspension was allowed to reach RT and was stirred for 4 h. EtOAc (60 mL) and H2O (10 mL) were added and the organic layer was isolated, washed with 50% brine (10 mL), dried (MgSO4), filtered and evaporated to leave a brown oil, which solidified upon standing (1.05 g). The solid was taken up in CH2Cl2 (4 mL) and purified by column chromatography on silica gel, eluting with EtOAc in CH2Cl2 (6%→40%), to give a white solid. Yield: 600 mg (45%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198279B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-1b800b78c88f466f99b47524793074aa
출처 메모uspto-grants-2012_06