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HRID 532170作成日:2026年10月26日

2,2,2-Trifluoroethanol → 1,3-Dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzene

https://huagongshe.com/reaction/532170

反応式

関与物質

役割名称HCID仕込み量
反応物2,2,2-TrifluoroethanolHCID 6409—
反応物Cesium carbonateHCID 10796—
反応物Ethyl 2-oxocyclohexanecarboxylateHCID 95543—
反応物Benzene, 1,3-dichloro-2-iodo-5-nitro-HCID 112948—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Ethyl AcetateHCID 8857—
生成物1,3-Dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzeneHCID 1385222726.4%

反応手順

A Mixture of Cs2CO3 (17.22 g, 52.84 mmol), CuBr (361 mg, 2.52 mmol) and ethyl 2-oxocyclohexanecarboxylate (856 mg, 5.03 mmol) in DMSO (30 mL) under N2 was stirred for 0.5 h at rt. Then a solution of 1,3-dichloro-2-iodo-5-nitrobenzene (8.0 g, 25.16 mmol) and 2,2,2-trifluoroethanol (3.02 g, 30.19 mmol) in DMSO (20 mL) was added to it. The reaction mixture was stirred at 80° C. for 18 h and cooled to room temperature, and then directly passed through celite. After rinsed with 250 ml of EA, the combined filter was washed by brine, dried over anhydrous Na2SO4, concentrated under reduced pressure. The residue was purified by column chromatography over silica gel eluted with PE:EA (100:1) to provide 1,3-dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzene (1.93 g, yield 12.6%) as pale yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853186B2
出典データセットuspto-grants-2014_10
ORD IDord-c2c96e8aeee44567aec83a1e90f1aa1b
出典メモuspto-grants-2014_10