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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1421369생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1421369

반응식

참여 물질

역할이름HCID투입량
반응물MethylparabenHCID 7456—
반응물Potassium CarbonateHCID 11430—
반응물Amyl AcetateHCID 12348—
반응물Thionyl ChlorideHCID 24386—
반응물1-(Piperidin-1-yl)ethanolHCID 3030541—
용매DichloromethaneHCID 6344—
생성물4-(2-Piperidinoethoxy)benzoic acid hydrochlorideHCID 574383568.1%

반응 조건

온도135 °C

반응 단계

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% .

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06075146
출처 데이터셋uspto-grants-2000_06
ORD IDord-b39922028e7646dc804bf6a6f1016d27
출처 메모uspto-grants-2000_06