戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1421371作成日:2026年10月26日

Methylparaben → 4-(2-Piperidinoethoxy)benzoic acid hydrochloride

https://huagongshe.com/reaction/1421371

反応式

関与物質

役割名称HCID仕込み量
反応物MethylparabenHCID 7456—
反応物Potassium CarbonateHCID 11430—
反応物2,2,2-Trifluoroethanesulfonyl chlorideHCID 74242—
反応物1-(Piperidin-1-yl)ethanolHCID 3030541—
溶媒DichloromethaneHCID 6344—
溶媒Amyl AcetateHCID 12348—
生成物4-(2-Piperidinoethoxy)benzoic acid hydrochlorideHCID 574383593.2%

反応条件

温度140 °C

反応手順

Into a 50 ml round bottom flask is placed 4.93 g (27.0 mmol) of 2,2,2-trifluoroethanesulfonyl chloride and 25 ml of methylene chloride. The resulting solution is cooled with an ice bath as 3.22 g (24.9 mmol) of 1-piperidinoethanol in 7 ml of methylene chloride is added dropwise. After the addition is complete, the ice bath is removed and the resulting slurry is stirred for about 12 hours. The reaction mixture is concentrated on a rotary evaporator to yield a waxy residue. The solid residue is slurried in 45 ml of amyl acetate and then potassium carbonate (5.50 g, 39.9 mmol) and methyl 4-hydroxybenzoate (2.26 g, 14.8 mmol) are added. The resulting mixture is heated to 140° C. for 2 hours. The reaction mixture is cooled to room temperature and washed twice with water and the organic layer is extracted with 10.5 ml of 8 N hydrochloric acid. The aqueous layer is heated at gentle reflux for 4 hours. The resulting slurry is cooled to 50° C. and 11 ml of acetone is added. The slurry is cooled to 0-5° C. and stirred for 1 hour. The product is filtered, washed with cold acetone, and dried at 50° C. in vacuo to yield 3.94 g of product, (90%). 1H NMR. HPLC 96.9%. TRS 2.78%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06075146
出典データセットuspto-grants-2000_06
ORD IDord-a468fc0052b347668176a6bfc4de27e6
出典メモuspto-grants-2000_06