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HRID 428213作成日:2026年10月26日

Methyl 4-trimethylsilylethynylbenzoate → Methyl 4-[3-oxo-3-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-1-propynyl]benzoate

https://huagongshe.com/reaction/428213

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-trimethylsilylethynylbenzoateHCID 640161—
反応物5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carbonyl chlorideHCID 2795466—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒DichloromethaneHCID 6344—
生成物Methyl 4-[3-oxo-3-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-1-propynyl]benzoateHCID 9799722—

反応手順

8.4 g (36 mmol) of 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthoyl chloride, 6.9 g (29.7 mmol) of methyl 4-trimethylsilylethynylbenzoate and 100 ml of dichloromethane are introduced into a round-bottomed flask. 16.8 g (125 mmol) of AlCl3 are added portionwise at 0° C. and the mixture is stirred at room temperature for 8 hours. The reaction medium is poured into ice and extracted with dichloromethane, and the organic phase is separated out after settling has taken place, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with a mixture of dichloromethane and hexane (50/50% by volume). 6.8 g (61%) of the expected product are collected, with a melting point of 113-4° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313162B1
出典データセットuspto-grants-2001_11
ORD IDord-e01264b5fb444276bc0a7c64dfa92a4d
出典メモuspto-grants-2001_11