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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1710600생성일: 2026년 10월 23일

tert-Butyl piperazine-1-carboxylate → HCID 67094789, 화합물

https://huagongshe.com/ko/reaction/1710600

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참여 물질

역할이름HCID투입량
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물Binap, (A+-)-HCID 634876—
반응물Sodium t-butoxideHCID 23676156—
반응물2-Bromo-4-nitro(trifluoromethoxy)benzeneHCID 24721641—
촉매palladium(II) acetateHCID 167845—
용매TolueneHCID 1140—
생성물HCID 67094789HCID 6709478959.2%

반응 조건

온도60 °C

반응 단계

A mixture of 0.048 g palladium(II)-acetate (0.214 mmol) and 0.133 g BINAP (0.214 mmol) in 7 mL toluene was heated to 60° C., stirred for 10 min. and the obtained suspension was added dropwise to a solution of 0.51 g 2-bromo-4-nitro-1-(trifluoromethoxy)benzene (1.783 mmol), 0.343 g tert.butyl-piperazine-1-carboxylate (1.842 mmol) and 0.232 g sodium tert-butoxide (2.414 mmol) in 8 mL of toluene. The thus obtained reaction mixture was treated at 130° C. for 1.5 h in a commercial microwave oven. The organic layer was washed with water, the aqueous phase was extracted with dichloromethane and the combined organic layers were extracted with saturated aqueous sodium chloride, dried over sodium sulfate, filtered, and the solvent was evaporated under reduced pressure. The crude product was further purified via silica gel chromatography using a ISCO Companion system (eluent cyclohexane-ethyl acetate 5-25%) to yield 0.413 g of product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07790727B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-33e18adf3c554e2bb7578855c5491576
출처 메모uspto-grants-2010_09