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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 736117생성일: 2026년 10월 25일

Tri-o-tolylphosphine → 4-(2-Chloro-4-trifluoromethylphenyl)piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/736117

반응식

참여 물질

역할이름HCID투입량
반응물Tri-o-tolylphosphineHCID 80271—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물3-Chloro-4-iodobenzotrifluorideHCID 2736612—
반응물Sodium t-butoxideHCID 23676156—
용매Diethyl EtherHCID 3283—
용매1,4-DioxaneHCID 31275—
생성물4-(2-Chloro-4-trifluoromethylphenyl)piperazine-1-carboxylic acid tert-butyl esterHCID 5348551810%

반응 조건

온도100 °C

반응 단계

A mixture of 0.5 g (1.6 mmol) of 3-chloro-4-iodobenzotrifluoride 0.7 g (3.8 mmol), N-Boc-piperazine, 41 mg (0.04 mmol) Tris(dibenzylideneacetone)dipalladium chloroform complex, 0.44 g (4.43 mmol) sodium-t-butoxide and 48 mg (0.16 mmol) tri-o-tolylphosphine in 6 ml dioxane was heated overnight at 100° C. The solution was allowed to cool to room temperature, taken up in ether (30 ml) and washed with brine (25 ml). The organic layer was dried over Na2SO4, filtered and the solvent was removed in vacuo. The crude oil was chromatographed over on silica gel: Eluent: Heptane-AcOEt 0-10% over 15 min to provide the title compound (0.06 g, 10%) as a brown oil, MS (m/e): 365.1 (MH+, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07595314B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-76b19fc017a945dbb8eb74112f1ddbd5
출처 메모uspto-grants-2009_09