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HRID 1191582作成日:2026年10月25日

Toluene → 4-(4'-Chloro-4-ethylbiphenyl-3-yl)-2-methoxymethyl-2,6,6-trimethylpyran-3,5-dione

https://huagongshe.com/reaction/1191582

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物ChloroformHCID 6212—
反応物2-Methoxymethyl-2,6,6-trimethylpyran-3,5-dioneHCID 68488092—
反応物HCID 178476534HCID 178476534—
溶媒Hydrochloric AcidHCID 313—
溶媒DichloromethaneHCID 6344—
生成物4-(4'-Chloro-4-ethylbiphenyl-3-yl)-2-methoxymethyl-2,6,6-trimethylpyran-3,5-dioneHCID 6848612523.9%

反応条件

温度80 °C

反応手順

To a mixture of 2-methoxymethyl-2,6,6-trimethylpyran-3,5-dione (0.141 g, 0.705 mmol) and N,N-dimethylaminopyridine (0.43 g, 3.52 mmol) in a mixed solvent system of anhydrous chloroform (7.5 ml) and anhydrous toluene (1.75 ml), is added 4′-chloro-4-ethylbiphenyl-3-yllead triacetate (0.465 g, 0.775 mmol) in one portion and the mixture heated at 80° C. for 2 hours. The mixture is allowed to cool to room temperature, diluted with dichloromethane and dilute aqueous hydrochloric acid, and stirred for 5 minutes then filtered through diatomaceous earth to remove inorganic residues (additional washing with solvents). The organic fractions are combined, dried over anhydrous magnesium sulfate, filtered and the filtrate is concentrated in vacuo. The residue is purified by column chromatography on silica gel (hexane/ethyl acetate 4:1 ratio). Fractions containing the desired product are combined and evaporated in vacuo. Trituration with hexanes affords 4-(4′-chloro-4-ethylbiphenyl-3-yl)-2-methoxymethyl-2,6,6-trimethylpyran-3,5-dione (0.070 g) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08680012B2
出典データセットuspto-grants-2014_03
ORD IDord-fe095421815c49c4939072c7f40fdd63
出典メモuspto-grants-2014_03