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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 856072생성일: 2026년 10월 24일

p-Bromochlorobenzene → Tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/856072

반응식

참여 물질

역할이름HCID투입량
반응물p-BromochlorobenzeneHCID 7806—
반응물Ethyl AcetateHCID 8857—
반응물4-Amino-1-Boc-piperidineHCID 1268291—
반응물Sodium t-butoxideHCID 23676156—
촉매palladium(II) acetateHCID 167845—
촉매Binap, (A+-)-HCID 634876—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물Tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylateHCID 149150386%

반응 단계

A mixture of p-bromochlorobenzene (1.91 g, 9.99 mmol), tert-butyl 4-aminopiperidine-1-carboxylate (2.0 g, 9.99 mmol), palladium acetate (45 mg, 0.2 mmol), (R)-(+)-BINAP (187 mg, 0.3 mmol) and sodium tert-butoxide (1.35 g, 14.0 mmol) in toluene (20 ml) was refluxed under a nitrogen atmosphere for 1 hour. Ethyl acetate and water were added to the reaction mixture while stirring, the insoluble substances were removed by filtration through Celite, and the filtrate was then extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, and then filtered. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (methylene chloride/methanol=100/1) to afford tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylate (2.67 g, yield 86%) as a yellow powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07262212B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-c276d8dff44d4683981ae2411bdadb15
출처 메모uspto-grants-2007_08