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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 611036생성일: 2026년 10월 27일

Thiophene → Ethyl 4-[(5,5-dimethyl-8-(2-thienyl)-5,6-dihydronaphthalen-2-yl)azo]benzoate

https://huagongshe.com/reaction/611036

반응식

참여 물질

역할이름HCID투입량
반응물ThiopheneHCID 8030—
반응물Ethyl 4-[(5,6-dihydro-5,5-dimethyl-8-trifluoromethylsulfonyloxy-naphthalen-2-yl)azo]benzoateHCID 22323756—
반응물HCID 178418306HCID 178418306—
촉매ZincchlorideHCID 3007855—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매TetrahydrofuranHCID 8028—
용매Ammonium ChlorideHCID 25517—
생성물Ethyl 4-[(5,5-dimethyl-8-(2-thienyl)-5,6-dihydronaphthalen-2-yl)azo]benzoateHCID 13006282—

반응 단계

To a cold solution (-78° C.) of thiophene (0.07 ml, 0.75 mmol) in 1.5 ml of TBF was added t-BuLi (0.457 ml, 0.75 mmol, 1.7 M in pentane) and stirred for 2 h. To this solution, ZnCl2 (168 mg, 1.2 mmol) in 1.5 ml of THF was added. The resulting solution was warmed to room temperature, stirred for 1 h and was added (via cannula) to a solution of ethyl 4-[(5,6-dihydro-5,5-dimethyl-8-trifluoromethylsulfonyloxy-naphthalen-2-yl)azo]benzoate (Compound D11, 150 mg, 0.30 mmol) and tetrakis(triphenylphosphine)palladium(O) (10.6 mg) in 2.5 ml of THF. The resulting mixture was heated at 50° C. for 2.5 h. The reaction was diluted with sat. aqueous NH4Cl and extracted with ethyl acetate. The combined organic layer was dried over Na2SO4 and concentrated to an oil. The crude product was purified by flash chromatography (silica, ethyl acetate: hexane 5:95) to afford the title compound as a red foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05998655
출처 데이터셋uspto-grants-1999_12
ORD IDord-d027a9a430ec440a95a5cb28e4f80a03
출처 메모uspto-grants-1999_12