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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 469694생성일: 2026년 10월 25일

Potassium Carbonate → 4-(4-Chlorophenethyl)piperazin-2-one

https://huagongshe.com/reaction/469694

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Piperazin-2-oneHCID 231360—
반응물2-(4-Chlorophenyl)ethyl chlorideHCID 3790359—
용매Dimethyl SulfoxideHCID 679—
생성물4-(4-Chlorophenethyl)piperazin-2-oneHCID 5809222960.8%

반응 조건

온도85 °C

반응 단계

Piperazinone (1.04 g, 10.4 mmol), 1-chloro-4-(2-chloroethyl)benzene (2.28 g, 10.4 mmol) and K2CO3 (1.72 g, 12.4 mmol) were combined in DMSO (12 mL) and heated to 85° C. for 2 h. The mixture was partitioned between H2O (20 mL) and CH2Cl2 (20 mL), and the organic layer was removed. The aqueous layer was extracted with CH2Cl2 (3×20 mL), the combined organics were concentrated, and the residue was dissolved in 2 N HCl (50 mL). This acidic mixture was washed with CH2Cl2 (3×20 mL) and then made basic with 6 N NaOH. The basic mixture was extracted with CH2Cl2 (3×20 mL), and the extracts were combined, dried and concentrated to provide the title compound (1.51 g, 60%) as an orange solid: 1H NMR (500 MHz, DMSO-d6) δ 7.72 (s, 1H), 7.32 (d, J=8.8 Hz, 2H), 7.26 (d, J=8.8 Hz, 2H), 3.14-3.10 (m, 2H), 2.96 (s, 2H), 2.74 (t, J=6.6 Hz, 2H), 2.62-2.53 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629158B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-6ab992dd39dd40e9ae8c235631e560d4
출처 메모uspto-grants-2014_01