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HRID 53382作成日:2026年10月23日

4,4-Dimethyl-7-ethynyl-1-tetralone → Benzoic acid, 4-((5,6,7,8-tetrahydro-5,5-dimethyl-8-oxo-2-naphthalenyl)ethynyl)-, ethyl ester

https://huagongshe.com/ja/reaction/53382

反応式

関与物質

役割名称HCID仕込み量
反応物4,4-Dimethyl-7-ethynyl-1-tetraloneHCID 10750476—
反応物Ethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoateHCID 15345545—
生成物Benzoic acid, 4-((5,6,7,8-tetrahydro-5,5-dimethyl-8-oxo-2-naphthalenyl)ethynyl)-, ethyl esterHCID 3025901—

反応手順

Employing the same general procedure as for the preparation of ethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoate (Compound 1), 4 g (21.7 mmol ) of 7-ethynyl-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one (Compound L) was converted into the title compound using 6 g (21.7 mmol) of ethyl 4-iodobenzoate, 5 g (7.2 mmol) of bis(triphenylphosphine)palladium(II) chloride and 1.4 g (7.2 mmol) of cuprous iodide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05618931
出典データセットuspto-grants-1997_04
ORD IDord-43c2d0092e9e45ee9a564bd57c4bb551
出典メモuspto-grants-1997_04