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HRID 46295作成日:2026年10月25日

Dichloromethane → tert-butyl 4-(5-chloro-2-hydroxyphenyl)-1H-pyrazole-1-carboxylate

https://huagongshe.com/reaction/46295

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Potassium CarbonateHCID 11430—
反応物4-Chloro-2-iodophenolHCID 620234—
反応物tert-butyl 4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylateHCID 16217654—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物tert-butyl 4-(5-chloro-2-hydroxyphenyl)-1H-pyrazole-1-carboxylateHCID 5943651866%

反応条件

温度50 °C

反応手順

A suspension of 4-chloro-2-iodophenol (200 mg, 0.78 mmol) and potassium carbonate (434 mg, 3.14 mmol) in 1,4-dioxane (3 mL) and water (1 mL) was degassed and heated for 1 hour at 50° C. tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate (347 mg, 1.18 mmol) and palladium (0) tetrakis(triphenylphoshine) (91 mg, 0.08 mmol) were added and the mixture heated at 50° C. for 5 hours. Dichloromethane (20 ml) and water (10 ml) were added and the organics separated and evaporated in vacuo. The residue was purified by column chromatography (silica gel) eluting with ethyl acetate:heptane (2:8 to 1:0, by volume) to afford the title product as a white solid, 155 mg, 66% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541588B2
出典データセットuspto-grants-2013_09
ORD IDord-49e6dad53c78479fad1a4142b9f5c63e
出典メモuspto-grants-2013_09