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HRID 748729作成日:2026年10月25日

Hexane → 4-[1-(4-Chlorophenylsulfonyl)pentyl]pyridine

https://huagongshe.com/reaction/748729

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物Butyl iodideHCID 10962—
反応物4-(4-Chlorophenylsulfonylmethyl)pyridineHCID 23028643—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物4-[1-(4-Chlorophenylsulfonyl)pentyl]pyridineHCID 5975094163%

反応条件

温度-78 °C

反応手順

At −78° C., butyl lithium (a 1.57M hexane solution; 0.29 ml, 0.448 mmol) was added dropwise to a tetrahydrofuran (5 ml) solution of 4-(4-chlorophenylsulfonylmethyl)pyridine (100 mg, 0.374 mmol). At −78° C., the resulting mixture was stirred for 10 minutes. Iodobutane (51 μl, 0.448 mmol) was then added thereto. The temperature of the reaction mixture was gradually elevated to room temperature, at which stirring was performed for 16 hours. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with brine and then dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was subjected to flash chromatography on a silica gel column. The fraction obtained from the hexane:ethyl acetate (=2:1) eluate was concentrated under reduced pressure to give the title compound (76 mg, 63%) as a white solid. The resulting solid was washed with hexane-ether and then collected by filtration, whereby the title compound was obtained as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07399775B2
出典データセットuspto-grants-2008_07
ORD IDord-48108732bb5a4d088ae621ee67d288b9
出典メモuspto-grants-2008_07