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HRID 555429作成日:2026年10月27日

2-Tert-Butylphenol → 2-(2-Tert-butylphenoxy)-3-nitrothiophene

https://huagongshe.com/reaction/555429

反応式

関与物質

役割名称HCID仕込み量
反応物2-Tert-ButylphenolHCID 6923—
反応物Potassium CarbonateHCID 11430—
反応物2-Chloro-3-nitrothiopheneHCID 220186—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物2-(2-Tert-butylphenoxy)-3-nitrothiopheneHCID 59857371—

反応条件

温度105 °C

反応手順

To a solution of 2-chloro-3-nitrothiophene (1.13 g, 6.93 mmol) in NMP (10 mL) in a pressure vessel was added 2-tert-butylphenol (1.04 g, 6.93 mmol) and K2CO3 (1.0 g, 10.1 mmol). The reaction was flushed with nitrogen, sealed and then heated to 105° C. for 48 h. The reaction was cooled to rt, diluted with EtOAc (˜150 mL) and washed twice with saturated aqueous NaCl (2ט150 mL). The aqueous washes were then back extracted with EtOAc. The combined organics were dried over MgSO4, filtered and concentrated to yield the crude desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08053450B2
出典データセットuspto-grants-2011_11
ORD IDord-eb9dfcffa5234e0e81072bfdd967b62b
出典メモuspto-grants-2011_11