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HRID 76080作成日:2026年10月24日

Dimethyl Sulfoxide → [1-(4-Acetyl-phenyl)-piperidin-4-yl]-acetic acid ethyl ester

https://huagongshe.com/ja/reaction/76080

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物4'-FluoroacetophenoneHCID 9828—
反応物Ethyl 2-(piperidin-4-yl)acetateHCID 2760465—
溶媒Diethyl EtherHCID 3283—
生成物[1-(4-Acetyl-phenyl)-piperidin-4-yl]-acetic acid ethyl esterHCID 57442326—

反応条件

温度150 °C

反応手順

A microwave vial was charged with 4′-fluoroacetophenone (1.2 Ml, 10.4 mmol, 1.0 equiv) and 2-(piperidin-4-yl)-acetic acid ethyl ester (3.5 g, 20.7 mmol, 2.0 equiv) in 20 Ml DMSO. The homogeneous reaction was heated to 150° C. for 20 min. The cooled reaction was then diluted with ether and washed sequentially with saturated ammonium chloride, water, and brine. The organic extracts were then dried over sodium sulphate, filtered, and concentrated in vacuo. Purification by flash chromatography (10-40% EtOAc in hexanes) afforded the title compound: 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.32 (t, J=7.07 Hz, 3H) 1.47 (d, J=12.13 Hz, 2H) 1.62 (br.s., 1H) 1.90 (d, J=12.63 Hz, 2H) 2.04-2.15 (m, J=11.18, 11.18, 7.45, 7.45, 3.79, 3.66 Hz, 1H) 2.33 (d, J=7.07 Hz, 2H) 2.57 (s, 3H) 2.97 (td, J=12.57, 2.15 Hz, 2H) 3.93 (d, J=12.88 Hz, 2H) 4.20 (q, J=7.07 Hz, 2H) 6.96 (d, J=6.82 Hz, 2H) 7.92 (d, J=9.09 Hz, 2H); (M+H)+290.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835451B2
出典データセットuspto-grants-2014_09
ORD IDord-96dbcddc02ee40bf91e3618a3e3668a8
出典メモuspto-grants-2014_09