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HRID 1371作成日:2026年10月23日

Tri-o-tolylphosphine → Ethyl (E)-4-[-2-(5,6-dihydro-5,5-dimethyl-8-(ethylthio)-naphthalen-2-yl)ethenyl]benzoate

https://huagongshe.com/ja/reaction/1371

反応式

関与物質

役割名称HCID仕込み量
反応物Tri-o-tolylphosphineHCID 80271—
反応物Ethyl 4-vinylbenzoateHCID 10866858—
反応物2-Bromo-5,6-dihydro-5,5-dimethyl8-(ethylthio)-naphthaleneHCID 22571521—
触媒palladium(II) acetateHCID 167845—
溶媒TriethylamineHCID 8471—
生成物Ethyl (E)-4-[-2-(5,6-dihydro-5,5-dimethyl-8-(ethylthio)-naphthalen-2-yl)ethenyl]benzoateHCID 86586452—

反応条件

温度90 °C

反応手順

To a degassed solution of 0.50 g (1.7 mmol) of 2-bromo-5,6-dihydro-5,5-dimethyl-8-(ethylthio)-naphthalene (Compound A36) and 0.45 g (2.5 mmol) of ethyl 4-vinylbenzoate in 4.0 mL of triethylamine, was added 109 mg (0.36 mmol) of tri-o-tolylphosphine and then 35 mg (0.16 mmol) of palladium(II) acetate. The reaction was heated at 90° C. for 2.25 h. The reaction was concentrated in vacuo and purified by flash chromatography (silica, 2% ethyl acetate in hexane) to afford the title compound as a colorless oil.

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-b1bd58830652436484aeb0d21b29efe6
出典メモuspto-grants-1998_03