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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1421371생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1421371

반응식

참여 물질

역할이름HCID투입량
반응물MethylparabenHCID 7456—
반응물Potassium CarbonateHCID 11430—
반응물2,2,2-Trifluoroethanesulfonyl chlorideHCID 74242—
반응물1-(Piperidin-1-yl)ethanolHCID 3030541—
용매DichloromethaneHCID 6344—
용매Amyl AcetateHCID 12348—
생성물4-(2-Piperidinoethoxy)benzoic acid hydrochlorideHCID 574383593.2%

반응 조건

온도140 °C

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06075146
출처 데이터셋uspto-grants-2000_06
ORD IDord-a468fc0052b347668176a6bfc4de27e6
출처 메모uspto-grants-2000_06