돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1771944생성일: 2026년 10월 27일

Potassium Carbonate → tert-Butyl (2-((2-oxo-4-(trifluoromethyl)-2H-chromen-7-yl)oxy)ethyl)carbamate

https://huagongshe.com/reaction/1771944

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Sodium BicarbonateHCID 516892—
반응물tert-Butyl N-(2-bromoethyl)carbamateHCID 4103526—
반응물7-Hydroxy-4-trifluoromethylcoumarinHCID 5375667—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물tert-Butyl (2-((2-oxo-4-(trifluoromethyl)-2H-chromen-7-yl)oxy)ethyl)carbamateHCID 8669972187%

반응 조건

온도85 °C

반응 단계

To a solution of 7-hydroxy-4-(trifluoromethyl)-2H-chromen-2-one (213 mg, 0.925 mmol) in DMF (1.5 mL) was added tert-butyl (2-bromoethyl)carbamate (416 mg, 1.851 mmol) and K2CO3 (384 mg, 2.776 mmol) at r.t. After stirred at 85° C. for 12 hours, the reaction mixture treated with 10.0 mL of saturated aqueous NaHCO3 solution. The organic layer was separated and the aqueous layer was extracted with Ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by flash column chromatography using a 9:1 v/v Hexane:Ethyl acetate as solvent to afford title compound (300 mg, 87% yield) as a white solid. 1H NMR 300 MHz (CDCl3) δ 7.64 (d, J=6.0 Hz, 1H), 6.91 (m, 2H), 6.61 (s, 1H), 4.95 (s, 1H), 4.11 (m, 2H), 3.58 (m, 2H), 1.56 (s, 9H), HRMS (m/z): [M+H]+ calculated for C17H18F3NO5. found, 374.1207.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09249128B2
출처 데이터셋uspto-grants-2016_02
ORD IDord-461862c62f3b4aeeb3539bc59581e950
출처 메모uspto-grants-2016_02