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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1125생성일: 2026년 10월 25일

Magnesium → Ethyl 2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-anthryl)-4-thiophenecarboxylate

https://huagongshe.com/reaction/1125

반응식

참여 물질

역할이름HCID투입량
반응물MagnesiumHCID 5462224—
반응물5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-bromoanthraceneHCID 15293215—
반응물Ethyl 5-bromothiophene-3-carboxylateHCID 15293216—
촉매ZincchlorideHCID 3007855—
촉매NiCl2 dppeHCID 86609808—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-anthryl)-4-thiophenecarboxylateHCID 9821896—

반응 단계

A solution of 9.5 g (30 mmol) of 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-bromoanthracene was added dropwise to a suspension of 724 mg (30 mmol) of magnesium in 10 ml of THF. Once the addition was completed, the mixture was heated at reflux for one hour. At room temperature 4.1 g (30 mmol) of anhydrous zinc chloride were added and the mixture was stirred for one hour. 5.2 g (22 mmol) of ethyl 2-bromo-4-thiophenecarboxylate and 120 mg (0.22 mmol) of the complex NiCl2 /DPPE were then added successively and the mixture was maintained under stirring at room temperature for 12 hours. The reaction medium was poured into ice-cold water, extracted with ethyl ether, the organic phase decanted off, dried over magnesium sulfate and evaporated. The residue obtained was chromatographed on a silica column eluted with a mixture of hexane and dichloromethane (60/40). After evaporation of the solvents, 6.35 g (74%) of the expected ester of melting point 107°-108° C. were recovered.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723499
출처 데이터셋uspto-grants-1998_03
ORD IDord-5222a695140643c8a668e63555fad359
출처 메모uspto-grants-1998_03