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HRID 2783作成日:2026年10月24日

Methyl Ethyl Ketone → Ethyl 4-(2-Piperidinoethoxy)benzoate

https://huagongshe.com/ja/reaction/2783

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl Ethyl KetoneHCID 6569—
反応物EthylparabenHCID 8434—
反応物Potassium CarbonateHCID 11430—
反応物Piperidine, 1-(2-chloroethyl)-, hydrochlorideHCID 74826—
溶媒WaterHCID 962—
溶媒Ethyl acetate acetonitrile triethylamineHCID 86586431—
生成物Ethyl 4-(2-Piperidinoethoxy)benzoateHCID 9838504—

反応条件

温度80 °C

反応手順

A mixture of ethyl 4-hydroxybenzoate (8.31 g), 1-(2-chloroethyl)piperidine monohydrochloride (10.13 g), potassium carbonate (16.59 g), and methyl ethyl ketone (60 mL) was heated to 80° C. After one hour, the mixture was cooled to about 55° C. and treated with additional 1-(2-chloroethyl)piperidine mono-hydrochloride (0.92 g). The resulting mixture was heated to 80° C. The reaction was monitored by thin layer chromatography (TLC), using silica-gel plates and ethyl acetate/acetonitrile/triethylamine (10:6:1, v/v). Additional portions of 1-(2-chloroethyl)piperidine hydrochloride were added until the starting 4-hydroxybenzoate ester was consumed. Upon complete reaction, the reaction mixture was treated with water (60 mL) and allowed to cool to room temperature. The aqueous layer was discarded and the organic layer concentrated in vacuo at 40° C. and 40 mm Hg. The resulting oil was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731327
出典データセットuspto-grants-1998_03
ORD IDord-6f47bc261884491694bca9fab87d052d
出典メモuspto-grants-1998_03