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HRID 374002作成日:2026年10月25日

Water → HCID 54306210、化合物

https://huagongshe.com/reaction/374002

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-(2-Nitrophenyl)-3-buten-2-oneHCID 140761—
反応物HCID 178418244HCID 178418244—
触媒Ethyltriphenylphosphonium iodideHCID 78474—
溶媒Diethyl EtherHCID 3283—
生成物HCID 54306210HCID 5430621042%

反応条件

温度0 °C

反応手順

20.3 g of ethyltriphenylphosphonium iodide was suspended in 160 ml of diethyl ether. Thereto was dropwise added 29.4 ml of 1.5 M n-butyllithium hexane solution, in 2 minutes with stirring at 0° C. Then, the mixture was stirred at 20° C. for 1 hour. To the resulting mixture being maintained at 10°-15° C. was dropwise added a solution of 8.4 g of 4-(2-nitrophenyl)-3-buten-2-one dissolved in 40 ml of diethyl ether, in 30 minutes. The resulting mixture was stirred at 20° C. for 3 hours. Thereto was added 100 ml of water. The organic layer was separated. The aqueous layer was extracted with 100 ml of diethyl ether, and the extract was combined with the previously separated organic layer. The combined solution was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography (eluant: n-hexane/ethyl acetate=5/1) to obtain 3.8 g (yield: 42%) of 1-(3-methyl-1,3-pentadienyl)-2-nitrobenzene as a light yellow oily material.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05166204
出典データセットuspto-grants-1992_11
ORD IDord-d72a41a053c94a029ecd43037fb1cc66
出典メモuspto-grants-1992_11