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HRID 32168作成日:2026年10月25日

Toluene → 1-Nitro-2-(3,3,4,4-tetramethylcyclopent-1-enyl)benzene

https://huagongshe.com/reaction/32168

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Sodium CarbonateHCID 10340—
反応物(2-Nitrophenyl)boronic acidHCID 2773548—
反応物Trifluoromethanesulfonic acid 3,3,4,4-tetramethylcyclopent-1-enyl esterHCID 59769424—
触媒HCID 178418397HCID 178418397—
溶媒EthanolHCID 702—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium chloride; waterHCID 57417360—
生成物1-Nitro-2-(3,3,4,4-tetramethylcyclopent-1-enyl)benzeneHCID 2314178099.8%

反応条件

温度90 °C

反応手順

A mixture of the trifluoromethanesulfonic acid 3,3,4,4-tetramethylcyclopent-1-enyl ester (992 mg, 3.64 mmol) produced in Example (54a), 2-nitrophenylboronic acid (729 mg, 4.37 mmol), tetrakis(triphenylphosphine)palladium(0) (219 mg, 0.189 mmol), 2N aqueous solution of sodium carbonate (3.64 mL), toluene (12.5 mL) and ethanol (6.3 mL) was stirred for 6 hours at an external temperature of 90° C. under a nitrogen atmosphere. The reaction mixture was air-cooled to room temperature, and then ethyl acetate and brine were added and extraction was performed twice with ethyl acetate. The separated organic layer was dried over anhydrous sodium sulfate. The desiccant was filtered off and the filtrate was concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (ethyl acetate/heptane) to give 891 mg of the title compound as a light brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425554B2
出典データセットuspto-grants-2008_09
ORD IDord-9d1ee1ce6ed44d579d2fffaef459ebe4
出典メモuspto-grants-2008_09