戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2214848作成日:2026年10月27日

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

https://huagongshe.com/reaction/2214848

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物5-NitrosalicylaldehydeHCID 66808—
反応物Ethyl (2E)-4,4,4-trifluoro-2-butenoateHCID 5371261—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物ethyl 6-nitro-2-(trifluoromethyl)-2H-1-benzopyran-3-carboxylateHCID 21883718—

反応条件

温度60 °C

反応手順

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),

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07109211B2
出典データセットuspto-grants-2006_09
ORD IDord-00ded272e84c4ed6b94cc41ee04656c5
出典メモuspto-grants-2006_09