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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 658812생성일: 2026년 10월 27일

Tri-o-tolylphosphine → N-(3-(3-(3-ethyl-3-hydroxypentyl)phenyl)propyl)-2,2,2-trifluoroacetamide

https://huagongshe.com/reaction/658812

반응식

참여 물질

역할이름HCID투입량
반응물Tri-o-tolylphosphineHCID 80271—
반응물4-Ethynylheptan-4-olHCID 12383898—
반응물N-(3-(3-bromophenyl)propyl)-2,2,2-trifluoroacetamideHCID 57608389—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물N-(3-(3-(3-ethyl-3-hydroxypentyl)phenyl)propyl)-2,2,2-trifluoroacetamideHCID 86628449—

반응 조건

온도90 °C

반응 단계

To a degassed solution of N-(3-(3-bromophenyl)propyl)-2,2,2-trifluoroacetamide (10) (2.29 g, 7.4 mmol) and 4-ethynylheptan-4-ol (2.4 g, 18.5 mmol) in triethylamine (2 mL) and DMF (18 mL) was added PdCl2(PPh3)2 (0.130 g, 0.185 mmol), P(o-Tol)3 (0.113 g, 0.37 mmol), and CuI (0.070 g, 0.37 mmol). The resulting mixture was degassed and stirred under argon at 90° C. overnight. The mixture was cooled to room temperature and the solids were removed by filtration through Celite. The filtrate was partitioned between diethyl ether and water and the combined organics were washed with brine, dried over Na2SO4 and concentrated under reduced pressure. Purification by flash chromatography (6 to 50% EtOAc-hexanes gradient) gave N-(3-(3-(3-ethyl-3-hydroxypentyl)phenyl)propyl)-2,2,2-trifluoroacetamide (12) as an amber oil. Yield (2.6 g, 95%): 1H NMR (400 MHz, DMSO-d6) δ 9.40 (s, 1H), 7.18-7.29 (m, 4H), 3.16 (q, J=7.2 Hz, 2H), 2.56 (t, J=7.2 Hz, 2H), 1.76 (quint, J=7.2 Hz, 2H), 1.53-1.67 (m, 8H), 0.97 (t, J=7.2 Hz, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08076516B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-66d66befb4aa4fb0bd7a930a125db280
출처 메모uspto-grants-2011_12