戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 263676作成日:2026年10月27日

Hydrochloric Acid → (E)-3-(4-chlorophenyl)-6-(2-naphthyl)-5-hexen-2-one

https://huagongshe.com/reaction/263676

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium hydrideHCID 24758—
反応物1-(p-Chlorophenyl)acetoneHCID 79699—
反応物(E)-3-(2-naphthyl)-2-propenyl bromideHCID 22252145—
溶媒BenzeneHCID 241—
溶媒DimethylformamideHCID 6228—
生成物(E)-3-(4-chlorophenyl)-6-(2-naphthyl)-5-hexen-2-oneHCID 1903860078%

反応手順

2.56 g of p-chlorophenylacetone was dissolved in a mixed solution of 5 ml of dimethylformamide and 5 ml of benzene, and a dimethylformamide 8 ml/benzene 8 ml solution containing 0.62 g of 60% oily sodium hydride and 3.50 g of (E)-3-(2-naphthyl)-2-propenyl bromide, was added under cooling with ice with stirring, followed by stirring at room temperature for 2 hours. The reaction solution was acidified by an addition of 1N hydrochloric acid and extracted by an addition of water and ethyl ether. Then, the organic layer was washed with a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. The drying agent was filtered off, and then, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=5/1) to obtain 3.70 g of the above-identified compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05643958
出典データセットuspto-grants-1997_07
ORD IDord-397ef8e10d194d67a54872cfd2b6b3e6
出典メモuspto-grants-1997_07