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HRID 346271作成日:2026年10月24日

Methyl 4-Formylbenzoate → 3-(4-Carbomethoxyphenyl)-1-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-prop-2-en-1-one

https://huagongshe.com/ja/reaction/346271

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-FormylbenzoateHCID 15294—
反応物1-(5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)ethan-1-oneHCID 2747562—
溶媒MethanolHCID 887—
溶媒Sodium HydroxideHCID 14798—
生成物3-(4-Carbomethoxyphenyl)-1-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-prop-2-en-1-oneHCID 5422116958.4%

反応手順

138 g (0.6 mole) of 6-acetyl-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene and 98.5 g (0.6 mole) of methyl 4-formylbenzoate in a mixture of 16 g of sodium hydroxide and 690 ml of methanol were stirred for 16 hours at room temperature. The precipitated crystals were filtered off under suction and dried to give 132 g of 3-(4-carbomethoxyphenyl)-1-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-prop-2-en-1-one of melting point 89°-91° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05061705
出典データセットuspto-grants-1991_10
ORD IDord-dfcc00fa2adc4dc1ad87edb6f478853e
出典メモuspto-grants-1991_10