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HRID 880358作成日:2026年10月26日

p-Fluoronitrobenzene → 1-[2,4-Bis(methoxymethoxy)-6-(4-nitrophenoxy)phenyl]ethanone

https://huagongshe.com/reaction/880358

反応式

関与物質

役割名称HCID仕込み量
反応物p-FluoronitrobenzeneHCID 9590—
反応物Potassium CarbonateHCID 11430—
反応物1-[2-Hydroxy-4,6-bis(methoxymethoxy)phenyl]ethanoneHCID 10879697—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物1-[2,4-Bis(methoxymethoxy)-6-(4-nitrophenoxy)phenyl]ethanoneHCID 6675931052%

反応手順

To a stirred suspension of 1-[2-hydroxy-4,6-bis(methoxymethoxy)phenyl]ethanone (78 g, 298 mmol) and K2CO3 (45.3 g, 328 mmol) in DMSO (500 mL) and water (40 ml) was added 4-nitro-1-fluorobenzene (46.3 g, 328 mmol, 1.1 eq). After stirring for 15 min. at room temperature, the resulting suspension was heated for 6 hours at 55° C. After cooling, the dark solution was diluted with ethyl acetate (2000 mL) and thoroughly washed with 10% citric acid solution, then with brine and dried over Na2SO4. The solvent was removed and the residue was columned over silica gel eluting with cyclohexane/ethyl acetate 3/1, to provide the title compound (56 g, 52% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08993556B2
出典データセットuspto-grants-2015_03
ORD IDord-e370b93d25df41e0848e26659099a52e
出典メモuspto-grants-2015_03