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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 76080생성일: 2026년 10월 24일

Dimethyl Sulfoxide → [1-(4-Acetyl-phenyl)-piperidin-4-yl]-acetic acid ethyl ester

https://huagongshe.com/ko/reaction/76080

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물4'-FluoroacetophenoneHCID 9828—
반응물Ethyl 2-(piperidin-4-yl)acetateHCID 2760465—
용매Diethyl EtherHCID 3283—
생성물[1-(4-Acetyl-phenyl)-piperidin-4-yl]-acetic acid ethyl esterHCID 57442326—

반응 조건

온도150 °C

반응 단계

A microwave vial was charged with 4′-fluoroacetophenone (1.2 Ml, 10.4 mmol, 1.0 equiv) and 2-(piperidin-4-yl)-acetic acid ethyl ester (3.5 g, 20.7 mmol, 2.0 equiv) in 20 Ml DMSO. The homogeneous reaction was heated to 150° C. for 20 min. The cooled reaction was then diluted with ether and washed sequentially with saturated ammonium chloride, water, and brine. The organic extracts were then dried over sodium sulphate, filtered, and concentrated in vacuo. Purification by flash chromatography (10-40% EtOAc in hexanes) afforded the title compound: 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.32 (t, J=7.07 Hz, 3H) 1.47 (d, J=12.13 Hz, 2H) 1.62 (br.s., 1H) 1.90 (d, J=12.63 Hz, 2H) 2.04-2.15 (m, J=11.18, 11.18, 7.45, 7.45, 3.79, 3.66 Hz, 1H) 2.33 (d, J=7.07 Hz, 2H) 2.57 (s, 3H) 2.97 (td, J=12.57, 2.15 Hz, 2H) 3.93 (d, J=12.88 Hz, 2H) 4.20 (q, J=7.07 Hz, 2H) 6.96 (d, J=6.82 Hz, 2H) 7.92 (d, J=9.09 Hz, 2H); (M+H)+290.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835451B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-96dbcddc02ee40bf91e3618a3e3668a8
출처 메모uspto-grants-2014_09