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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1004569생성일: 2026년 10월 25일

Triethylamine → (+)-(3,5-Dimethylbenzoyl)-3-(3,4-dichlorophenyl)piperazine

https://huagongshe.com/reaction/1004569

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3,5-Dimethylbenzoic acidHCID 10356—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물2-(3,4-Dichlorophenyl)piperazineHCID 4231356—
용매DichloromethaneHCID 6344—
생성물(+)-(3,5-Dimethylbenzoyl)-3-(3,4-dichlorophenyl)piperazineHCID 1029215957.8%

반응 단계

To a cooled solution of CH2Cl2 (600 mL) containing 2-(3,4-dichlorophenyl)piperazine (6.934 g, 30 mmol), 3,5-dimethylbenzoic acid (4.55 g, 30 mmol), and N-hydroxybenzotriazole monohydrate (4.05 g, 30 mmol) at -20° C. were added Et3N (4.2 mL, 30 mmol) and N,N-dimethylaminopropylethylcarbodimide (DEC) (5.86 g, 30 mmol) under nitrogen. The reaction was kept at -20° C. for an hour and gradually warmed to RT overnight. After stirring 22 hours, the reaction was complete and CH2Cl2 (200 mL) was added. The organic solution was washed with brine (150 mL, 3×), dried over MgSO4, filtered and concentrated under vacuum to give 8.2 g of crude product. The product was crystallized from CH2Cl2 /Hexane to give a light yellow solid (6.3 g, 17.34 mmol, 57.8%). Mm.p.139-141° C.; FAB MS [M+1]+35Cl 363.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06051575
출처 데이터셋uspto-grants-2000_04
ORD IDord-f83c28f0b5ee407aa13c4f0398fad8a3
출처 메모uspto-grants-2000_04