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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45698생성일: 2026년 10월 25일

1,3-Dibromobenzene → tert-Butyl 4-(3-bromophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/45698

반응식

참여 물질

역할이름HCID투입량
반응물1,3-DibromobenzeneHCID 7927—
반응물Potassium CarbonateHCID 11430—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물L-ProlineHCID 145742—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Dimethyl SulfoxideHCID 679—
생성물tert-Butyl 4-(3-bromophenyl)piperazine-1-carboxylateHCID 10882380—

반응 단계

Into a 250-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed copper(I) iodide (1.0 g, 5.26 mmol, 0.20 equiv), L-proline (930 mg, 8.09 mmol, 0.30 equiv) in DMSO (50 mL). The resulting solution was stirred for 15 min at room temperature. Then, tert-butyl piperazine-1-carboxylate (5 g, 26.88 mmol, 1.00 equiv), 1,3-dibromobenzene (9.5 g, 40.25 mmol, 1.50 equiv), potassium carbonate (7.4 g, 53.62 mmol, 1.99 equiv) was added. The resulting solution was stirred overnight at 90° C. The reaction was then quenched by the addition of 100 mL of water. The resulting solution was extracted with 2×100 mL of ethyl acetate and the organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:6). This resulted in 2.9 g of tert-butyl 4-(3-bromophenyl)piperazine-1-carboxylate as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541448B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-c64ae6e5d8b24249b350bd014dc70f64
출처 메모uspto-grants-2013_09