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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1381884생성일: 2026년 10월 27일

Triethylamine → 1-(3-Acetylaminobenzoyl)-4-[2-(4-chlorophenyl)ethyl]piperazine

https://huagongshe.com/reaction/1381884

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물3-Acetamidobenzoic acidHCID 48847—
반응물1-[2-(4-Chlorophenyl)ethyl]piperazineHCID 12235714—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물1-(3-Acetylaminobenzoyl)-4-[2-(4-chlorophenyl)ethyl]piperazineHCID 19099536—

반응 단계

10 g of 3-acetamidobenzoic acid are dissolved in 100 ml of DMF. At a temperature of from -5° to 0° there are added dropwise, while stirring, firstly 5.65 g of triethylamine and then 6.05 g of chloroformic acid ethyl ester dissolved in 40 ml of CH2Cl2. The whole is stirred for a further 30 minutes at from 0° to +5° and then, at the same temperature, 12.54 g of 1-(p-chlorophenethyl)piperazine in 75 ml of DMF are added dropwise. The whole is stirred overnight at room temperature and then concentrated to dryness by evaporation. The residue is taken up in 350 ml of CH2Cl2 and the whole is washed with 150 ml of 2N NaOH and with 50 ml of H2O and dried over Na2SO4. After filtration and concentration by evaporation, a brown oil is obtained, which is caused to crystallise with ether. Recrystallisation is effected from ethanol/ether. 1-[2-(p-chlorophenyl)-ethyl]-4-(3-acetamidobenzoyl)-piperazine having a melting point of 101°-107° is thus obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04804661
출처 데이터셋uspto-grants-1989_02
ORD IDord-93c2324ff7574cbdb668543b2741734c
출처 메모uspto-grants-1989_02