戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1376作成日:2026年10月23日

Toluene → Ethyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-naphth-7-yl]naphth-2-oate

https://huagongshe.com/ja/reaction/1376

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Ethyl AcetateHCID 8857—
反応物Ethyl 6-bromonaphthalene-2-carboxylateHCID 1249959—
反応物(5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic acidHCID 22571498—
溶媒MethanolHCID 887—
溶媒HexaneHCID 8058—
溶媒Sodium CarbonateHCID 10340—
生成物Ethyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-naphth-7-yl]naphth-2-oateHCID 22571563—

反応条件

温度80 °C

反応手順

To a degassed solution of 0.39 g (1.4 mmol) of ethyl 6-bromo-naphthalene-2-carboxylate and 3.0 mL of toluene, was added sequentially 49 mg (0.04 mmol) of tetrakis-triphenylphosphine palladium(0), 2.0 mL (2.0 mmol) of 1M sodium carbonate and then a solution of 0.32 g (1.6 mmol) of (5,6,7,8-tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid (Compound B13) in 3.0 mL of MeOH. The reaction was heated at 80° C. for 6 h, diluted with 2N Na2CO3, and extracted with CH2Cl2 (2×), the organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. Flash chromatography (silica, 5% ethyl acetate in hexane) of the crude material gave the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723666
出典データセットuspto-grants-1998_03
ORD IDord-97b20453788c4bc8828b820164729c18
出典メモuspto-grants-1998_03