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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50864생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/50864

반응식

참여 물질

역할이름HCID투입량
반응물Methyl Ethyl KetoneHCID 6569—
반응물EthylparabenHCID 8434—
반응물Potassium CarbonateHCID 11430—
반응물Piperidine, 1-(2-chloroethyl)-, hydrochlorideHCID 74826—
용매WaterHCID 962—
용매Ethyl acetate acetonitrile triethylamineHCID 86586431—
생성물Ethyl 4-(2-Piperidinoethoxy)benzoateHCID 9838504—

반응 조건

온도80 °C

반응 단계

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 are added until the starting 4-hydroxybenzoate ester is 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713494B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-ae3cb0dae3e944c48580e55737574b4a
출처 메모uspto-grants-2004_03