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HRID 1421369作成日:2026年10月26日

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

https://huagongshe.com/reaction/1421369

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Amyl AcetateHCID 12348—
反応物Thionyl ChlorideHCID 24386—
反応物1-(Piperidin-1-yl)ethanolHCID 3030541—
溶媒DichloromethaneHCID 6344—
生成物4-(2-Piperidinoethoxy)benzoic acid hydrochlorideHCID 574383568.1%

反応条件

温度135 °C

反応手順

Into a 500 ml round bottom flask is placed 23.38 g (197 mmol) of thionyl chloride and 140 ml of methylene chloride. The resulting solution is cooled with an ice bath as 21.91 g (170 mmol) of 1-piperidinoethanol in 30 ml of methylene chloride is added over 30 minutes. After the addition is complete, the ice bath is removed and the mixture is stirred for about 12 hours. The reaction mixture is concentrated on a rotary evaporator to yield a solid residue. Amyl acetate (225 ml), potassium carbonate (34.4 g, 249 mmol), and methyl 4-hydroxybenzoate (14.1 g, 92 mmol) are added to the residue. The resulting slurry is heated to 135° C. for 5 hours. The reaction mixture is cooled to room temperature and washed twice with 100 ml of water. The organic layer is extracted with 53 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 50 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 17.9 g of product, (67%). 1H NMR. Compares to reference solution: HPLC potency 97.9%, TRS 1.50% .

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-b39922028e7646dc804bf6a6f1016d27
出典メモuspto-grants-2000_06