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HRID 629373作成日:2026年10月27日

Water → methyl 4-cyano-2-hydroxy-3-methyl-5-[4-(1H-pyrazol-1-yl)benzyl]benzoate

https://huagongshe.com/reaction/629373

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1-[4-(chloromethyl)phenyl]-1H-pyrazoleHCID 7130887—
反応物Tripotassium phosphate trihydrateHCID 18407952—
反応物Methyl 4-cyano-2-hydroxy-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoateHCID 131735370—
触媒HCID 178418807HCID 178418807—
溶媒1,4-DioxaneHCID 31275—
生成物methyl 4-cyano-2-hydroxy-3-methyl-5-[4-(1H-pyrazol-1-yl)benzyl]benzoateHCID 11846838422.5%

反応条件

温度90 °C

反応手順

To a solution of methyl 4-cyano-2-hydroxy-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (3.50 g) in 1,4-dioxane (30.0 mL) were added 1-(4-(chloromethyl)phenyl)-1H-pyrazole (2.12 g), tripotassium phosphate trihydrate (5.90 g) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) dichloromethane adduct (0.34 g), and the mixture was stirred at 90° C. for 16 hr under nitrogen atmosphere. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by flash silica gel column chromatography (ethyl acetate/petroleum ether) to give the title compound (0.86 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09315458B2
出典データセットuspto-grants-2016_04
ORD IDord-520b65b2fb3841b8a9cfc28f5e296dbf
出典メモuspto-grants-2016_04