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HRID 52857作成日:2026年10月24日

Citric Acid → 4-(3,4-Dichlorophenyl)-3-(4-dimethoxymethylphenyl)-2-butanone

https://huagongshe.com/ja/reaction/52857

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物3,4-Dichlorobenzyl chlorideHCID 7609—
反応物Sodium hydrideHCID 24758—
反応物4-DimethoxymethylphenylacetoneHCID 19073682—
溶媒BenzeneHCID 241—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物4-(3,4-Dichlorophenyl)-3-(4-dimethoxymethylphenyl)-2-butanoneHCID 1907373146%

反応手順

0.15 g of 60% oily sodium hydride was dissolved in a liquid mixture of 1.5 ml of dimethylformamide and 1.5 ml of benzene, and a dimethylformamide 2 ml/benzene 2 ml solution of 0.72 g of 4-dimethoxymethylphenylacetone was dropwise added thereto with stirring under cooling with ice. The mixture was stirred at the same temperature for 15 minutes. To this solution, a dimethylformamide 2 ml/benzene 2 ml solution of 0.65 ml of 3,4-dichlorobenzyl chloride was dropwise added with stirring under cooling with ice. The mixture was stirred at the same temperature for 40 minutes. Then, a 3% citric acid aqueous solution and ethyl ether were added for liquid separation. The organic layer was collected by separation, then washed with a saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure. The residue was subjected to medium pressure liquid chromatography (Lobar column™, size B, Lichroprep™ Si60F, manufactured by Merck Co.; hexane/ethyl acetate=10/1→6/1) to obtain 0.64 g (yield: 46%) of 4-(3,4-dichlorophenyl)-3-(4-dimethoxymethylphenyl)-2-butanone as colorless oily substance.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616803
出典データセットuspto-grants-1997_04
ORD IDord-43d94b084fa544dd890dfe8561624ccc
出典メモuspto-grants-1997_04