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HRID 395585作成日:2026年10月24日

Fluorobenzene → Methyl 6-(4-fluorophenyl)-6-oxohexanoate

https://huagongshe.com/ja/reaction/395585

反応式

関与物質

役割名称HCID仕込み量
反応物FluorobenzeneHCID 10008—
反応物Methyl 6-chloro-6-oxohexanoateHCID 520737—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Methyl 6-(4-fluorophenyl)-6-oxohexanoateHCID 69905189—

反応条件

温度-5 °C

反応手順

A suspension of 2.59 g (19.4.10−3 mol) of aluminum chloride in 4 ml of dichloromethane is prepared. It is cooled to −5° C. and a mixture of 0.97 ml (10.3.10−3 mol) of fluorobenzene and 1.31 ml (8.4.10−3 mol) of methyl 6-chloro-6-oxohexanoate in 3 ml of dichloromethane is added gradually, the temperature being maintained between −4 and −7° C. The temperature is then allowed to rise to 20° C. and, after 15 hours, the mixture is hydrolyzed in acidified iced water. It is extracted with dichloromethane and the organic phase obtained is washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The 2 g of crude product recovered in this way are purified by chromatography on silica gel using a petroleum ether/ethyl acetate mixture (96/4) as the eluent to give 1.26 g of the expected product in the form of a white powder (yield=63%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06605633B1
出典データセットuspto-grants-2003_08
ORD IDord-4a0976bcd5cf4adeb77cbdd025bb3b9f
出典メモuspto-grants-2003_08