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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 263676생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/263676

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물1-(p-Chlorophenyl)acetoneHCID 79699—
반응물(E)-3-(2-naphthyl)-2-propenyl bromideHCID 22252145—
용매BenzeneHCID 241—
용매DimethylformamideHCID 6228—
생성물(E)-3-(4-chlorophenyl)-6-(2-naphthyl)-5-hexen-2-oneHCID 1903860078%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05643958
출처 데이터셋uspto-grants-1997_07
ORD IDord-397ef8e10d194d67a54872cfd2b6b3e6
출처 메모uspto-grants-1997_07