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HRID 1125作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/1125

反応式

関与物質

役割名称HCID仕込み量
反応物MagnesiumHCID 5462224—
反応物5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-bromoanthraceneHCID 15293215—
反応物Ethyl 5-bromothiophene-3-carboxylateHCID 15293216—
触媒ZincchlorideHCID 3007855—
触媒NiCl2 dppeHCID 86609808—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-anthryl)-4-thiophenecarboxylateHCID 9821896—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723499
出典データセットuspto-grants-1998_03
ORD IDord-5222a695140643c8a668e63555fad359
出典メモuspto-grants-1998_03