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HRID 2214848생성일: 2026년 10월 26일

Potassium Carbonate → ethyl 6-nitro-2-(trifluoromethyl)-2H-1-benzopyran-3-carboxylate

https://huagongshe.com/reaction/2214848

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물5-NitrosalicylaldehydeHCID 66808—
반응물Ethyl (2E)-4,4,4-trifluoro-2-butenoateHCID 5371261—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물ethyl 6-nitro-2-(trifluoromethyl)-2H-1-benzopyran-3-carboxylateHCID 21883718—

반응 조건

온도60 °C

반응 단계

A mixture of 5-nitrosalicylaldehyde (4.80 g, 28.7 mmol) and ethyl 4,4,4-trifluorocrotonate (6.6 g, 39.4 mol) in anhydrous DMF was warmed to 60° C. and treated with anhydrous K2CO3 (3.90 g, 28.9 mol). The solution was maintained at 60° C. for 20 hours, cooled to room temperature, diluted with water, and extracted with ethyl acetate. The organic extracts were washed with brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo to afford an oil. The oil was dissolved in diethyl ether (5 mL). Hexanes was added until the solution became cloudy. Upon standing at room temperature overnight the ester was obtained as yellow crystals (0.856 g, 7% yield). This material was of sufficient purity to be used in subsequent steps without further purification. 1H NMR (CDCl3/300 MHz) 8.15–8.19 (m, 2H), 7.74 (s, 1H), 7.09 (d, 1H, J=8.9 Hz), 5.81 (q, 1H, J=5.8 Hz), 4.29–4.39 (m, 2H), 1.35 (t, 3H, J=6.0 Hz),

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07109211B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-00ded272e84c4ed6b94cc41ee04656c5
출처 메모uspto-grants-2006_09