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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241332생성일: 2026년 10월 26일

1,4-Dioxane → 1-(4-Chlorobenzoyl)piperazine

https://huagongshe.com/reaction/241332

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물tert-Butyl 4-(4-chlorobenzoyl)piperazine-1-carboxylateHCID 49814251—
용매DichloromethaneHCID 6344—
생성물1-(4-Chlorobenzoyl)piperazineHCID 410148499%

반응 단계

4-(4-Chloro-benzoyl)-piperazine-1-carboxylic acid tert-butyl ester (26 g) was dissolved in CH2Cl2 (350 mL). 4M HCL/Dioxane (150 mL) was added. The mixture was stirred at RT for 4 h. White precipitate was formed. The mixture was concentrated. The white solid was washed with Et2O. After the white solid was treated with 1N NaOH (200 mL) and extracted with Ethyl acetate (3×100 mL), the combined organic phase was dried over Na2SO4 and concentrated to give 17.79 g of desired product (99% yield). 1H-NMR (for HCl salt) (300 MHz, MeOD): δ 2.80-2.90 (m, 4H), 3.20-3.80 (m, 4H), 7.29-7.36 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08648197B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-97d7bd9150eb4f0f87feb48ae598b1c9
출처 메모uspto-grants-2014_02