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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1008866생성일: 2026년 10월 27일

Triethylamine → 1-(3-Biphenyl-3-yl-1,1-dimethylprop-2-yn-1-yl)-4-(2,2-dimethylpropanoyl)piperazine

https://huagongshe.com/reaction/1008866

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-BromobiphenylHCID 16449—
반응물1-(2,2-Dimethylpropanoyl)-4-(1,1-dimethylprop-2-yn-1-yl)piperazineHCID 86610208—
촉매TriphenylphosphineHCID 11776—
촉매Bis(triphenylphosphine)palladiumHCID 10122028—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-(3-Biphenyl-3-yl-1,1-dimethylprop-2-yn-1-yl)-4-(2,2-dimethylpropanoyl)piperazineHCID 6730575961.7%

반응 단계

1.05 g (4.5 mmol) of 3-bromobiphenyl and 0.9 g (3.6 mmol) of 1-(2,2-dimethylpropanoyl)-4-(1,1-dimethylprop-2-yn-1-yl)piperazine, prepared in step 5.1., 0.75 ml (5.38 mmol) of triethylamine and 0.028 g (0.11 mmol) of triphenylphosphine are dissolved in 8 ml of tetrahydrofuran. Under an argon atmosphere, 0.126 g (0.18 mmol) of the dichloride complex of bis(triphenylphosphine) palladium is added. The mixture is stirred for 15 minutes and then 0.014 g (0.07 mmol) of cuprous iodide is added. The mixture is stirred at ambient temperature for 4 hours and then at 60° C. overnight. After cooling to temperature it is diluted with 25 ml of ethyl acetate and filtered on paper. The solid is rinsed with 4 times 10 ml of ethyl acetate. 4 g of silica are added to the filtrate, which is evaporated to dryness. The residue is purified by chromatography on silica gel, eluting with a 90/10 then 80/20 and 70/30 mixture of cyclohexane and ethyl acetate, to give 0.90 g (2.22 mmol) of product in the form of a orange-colored oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07973042B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-72c1a8ef385746afa76eeaa09f3a3efc
출처 메모uspto-grants-2011_07