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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 713431생성일: 2026년 10월 26일

Ethyl bromoacetate → [4-(4-Chloro-benzoyl)-piperidin-1-yl]-acetic acid ethyl ester

https://huagongshe.com/reaction/713431

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물TriethylamineHCID 8471—
반응물4-(4-Chlorobenzoyl)PiperidineHCID 2777115—
용매AcetonitrileHCID 6342—
생성물[4-(4-Chloro-benzoyl)-piperidin-1-yl]-acetic acid ethyl esterHCID 7122696581.6%

반응 조건

온도85 °C

반응 단계

To a suspension of (4-chloro-phenyl)-piperidin-4-yl-methanone (1.0 g, 3.8 mmol) and bromo-acetic acid ethyl ester (0.71 g, 4.2 mmol) in acetonitrile (10 mL) was added triethylamine (0.78 g, 7.7 mmol), the reaction mixture was stirred at 85° C. for 15 h. The reaction mixture was cooled to ambient temperature, the solvent was removed, the residue was redissolved in DCM (20 mL), washed with water (20 mL), the organic layers were then washed with brine (20 mL) and dried over Na2SO4. Purification by flash chromatography gave the title compound as a white solid (1.01 g, 3.10 mmol, 81% yield). MS (ESI) m/z 310.3 (M+H+); HPLC (Novapak 150×3.9 mm C-18 column: mobile phase: 35-90% acetonitrile/water with 0.1% TFA, at 2 mL/min over 2 min.) t 1.45 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181266B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-b93deea389a9414db218e841e0a52304
출처 메모uspto-grants-2015_11