戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1239作成日:2026年10月23日

Ethyl 4-[(7,8-dihydro-5-hydroxy-8,8-dimethyl-5-carboethoxymethylnaphth-2-yl)ethynyl]benzoate → Trimethylsilylethyl 4-[(5,6,7,8,-tetrahydro-5-hydroxy-8,8-dimethyl-5-carboethoxymethylnaphth-2-yl)ethynyl]benzoate

https://huagongshe.com/ja/reaction/1239

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 4-[(7,8-dihydro-5-hydroxy-8,8-dimethyl-5-carboethoxymethylnaphth-2-yl)ethynyl]benzoateHCID 18314576—
反応物(Trimethylsilyl)ethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoateHCID 54412444—
生成物Trimethylsilylethyl 4-[(5,6,7,8,-tetrahydro-5-hydroxy-8,8-dimethyl-5-carboethoxymethylnaphth-2-yl)ethynyl]benzoateHCID 23361330—

反応手順

Employing the same general procedure as for the preparation of ethyl 4-[(5,6,7,8-tetrahydro-5-hydroxy-8,8-dimethyl-5-carboethoxymethylnaphth-2-yl)ethynyl]benzoate (Compound 113), 0.38 g (0.89 mmol) of trimethylsilylethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoate (Compound 116), was converted into the title compound (yellow solid) using 0.50 g (7.65 mmol) of zinc, 0.20 ml (1.78 mmol) of ethyl bromoacetate and 20 ml of dry benzene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723620
出典データセットuspto-grants-1998_03
ORD IDord-c1a4e1e535804129a0f31d37c5904ccb
出典メモuspto-grants-1998_03