돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 444793생성일: 2026년 10월 25일

Potassium Carbonate → Tert-butyl 3-(4,6-bistrifluoromethylpyridin-2-yl)propylcarbamate

https://huagongshe.com/reaction/444793

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물9-Borabicyclo(3.3.1)nonaneHCID 78966—
반응물tert-butyl N-(prop-2-en-1-yl)carbamateHCID 4067274—
반응물Pyridine, 2-bromo-4,6-bis(trifluoromethyl)-HCID 85875928—
촉매palladium(II) acetateHCID 167845—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 3-(4,6-bistrifluoromethylpyridin-2-yl)propylcarbamateHCID 8665069474%

반응 단계

To a stirred solution of tert-butyl allylcarbamate (1.95 g, 12.4 mmol) in THF (12 mL), 0.5 mol/L 9-borabicyclo[3.3.1]nonane (29.8 mL, 14.9 mmol) was added under argon atmosphere at room temperature. After stirred at room temperature for 4 h, a solution of 2-bromo-4,6-bistrifluoromethylpyridine (3.65 g, 12.4 mmol) in DMF (12 mL), Pd(OAc)2 (278 mg, 1.24 mmol), DPPF (859 mg, 1.55 mmol) and K2CO3 (2.92 g, 21.1 mmol) were added to the reaction mixture and stirred at room temperature for 7 h. To the reaction mixture, water was added and the crude product was extracted with EtOAc, washed with brine, dried over NaSO4 and the solvent was removed in vacuo. The crude product was purified by column chromatography (Hexane:EtOAc 10:1→2:1) to yield tert-butyl 3-(4,6-bistrifluoromethylpyridin-2-yl)propylcarbamate (3.41 g, 74%) as a colorless solid. 1H NMR (CDCl3, 400 MHz) δ 1.44 (9H, s), 1.96-2.03 (2H, m), 2.98-3.02 (2H, m), 3.20-3.25 (2H, m), 4.71 (1H, brs), 7.59 (1H, s), 7.72 (1H, s). CIMS (+) 373 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08476261B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-a2417668deaa487fb23f75a774839b97
출처 메모uspto-grants-2013_07