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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1795599생성일: 2026년 10월 27일

Cesium carbonate → 4-(5,8,8-Trimethyl-7,8-dihydro-naphthalen-2-yl-amino)-benzoic acid ethyl ester

https://huagongshe.com/reaction/1795599

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Ethyl 4-bromobenzoateHCID 22043—
반응물Bis(diphenylphosphino)-1,1'-binaphthylHCID 18630801—
반응물5,8,8-Trimethyl-7,8-dihydro-naphthalen-2-ylamineHCID 22218345—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물4-(5,8,8-Trimethyl-7,8-dihydro-naphthalen-2-yl-amino)-benzoic acid ethyl esterHCID 21024367—

반응 조건

온도100 °C

반응 단계

General Procedure L To a solution of 5,8,8-trimethyl-7,8-dihydro-naphthalen-2-yl-amine (Compound 64, 0.33 g, 1.8 mmol) and ethyl 4-bromobenzoate (0.52 g, 2.3 mmol) in 10.0 mL of toluene while stirring under argon were added cesium carbonate (0.89 g, 2.7 mmol), tris(dibenzylideneacetone)dipalladium(0) (Pd2(dba)3, 33 mg, 0.04 mmol) and bis(diphenylphosphino)-1,1′-binaphthyl (BINAP, 47 mg, 0.08 mmol) consecutively. The reaction was then heated at 100° C. for 24 h. The reaction was then cooled to room temperature, diluted with water and extracted 2 times with ethyl ether. The combined organic extracts were washed with brine, dried over MgSO4, filtered, and the solvents were removed in vacuo. The crude product was purified by silica gel chromatography (10% ethyl acetate in hexanes) to give the title compound as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07026487B2
출처 데이터셋uspto-grants-2006_04
ORD IDord-079a93512d444eb4a575adc250df4e07
출처 메모uspto-grants-2006_04