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HRID 2372506作成日:2026年10月27日

Toluene → Methyl 4-(4-phenoxyphenoxy)benzoate

https://huagongshe.com/reaction/2372506

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Methyl 4-nitrobenzoateHCID 12083—
反応物4-PhenoxyphenolHCID 13254—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DimethylformamideHCID 6228—
生成物Methyl 4-(4-phenoxyphenoxy)benzoateHCID 1987620182%

反応手順

Methyl 4-(4-phenoxyphenoxy)benzoate is synthesized as follows. A mixture of 15.00 g (80.6 mmoles) of 4-phenoxyphenol, 130 ml of N,N-dimethylformamide and 75 ml of toluene is agitated under nitrogen atmosphere. Potassium t-butoxide (9.32 g, 80.6 mmoles) is added with vigorous stirring and the mixture is heated to reflux. An azeotrope of t-butanol and toluene (85 ml) is collected at temperatures of 120° C. to 135° C. and is discarded. The mixture is cooled to ambient temperature, and a solution of 14.59 g (80.6 mmoles) of methyl 4-nitrobenzoate in 30 ml of N,N-dimethylformamide is added over a period of 15 minutes with cooling in a water bath. The mixture is heated at 100° C. for 14 hours, cooled to 20° C., and quenched with 1500 ml of ice water. The precipitate is filtered, dried in air and dissolved in 500 ml of acetone. The solution is filtered to remove insolubles, and the filtrate is concentrated by evaporation and cooled to precipitate methyl 4-(4-phenoxyphenoxy)benzoate. The recovered product weighs 21.23 g (82 percent yield) and has a melting point of 114° C. as determined by DSC.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05098985
出典データセットuspto-grants-1992_03
ORD IDord-a826ae7435d34e2ea88cc4fd001a5044
出典メモuspto-grants-1992_03