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HRID 733127作成日:2026年10月27日

Citric Acid → 5-tert-butyl-1-(2'-chloro-1,1'-biphenyl-3-yl)-1H-pyrazole-3-carboxylic acid

https://huagongshe.com/reaction/733127

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物Sodium CarbonateHCID 10340—
反応物TriphenylphosphineHCID 11776—
反応物Sodium HydroxideHCID 14798—
反応物2-Chlorophenylboronic acidHCID 2734322—
反応物ethyl 1-(3-bromophenyl)-5-tert-butyl-1H-pyrazole-3-carboxylateHCID 57428253—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒1-PropanolHCID 1031—
生成物5-tert-butyl-1-(2'-chloro-1,1'-biphenyl-3-yl)-1H-pyrazole-3-carboxylic acidHCID 11279690—

反応手順

To a solution of ethyl 1-(3-bromophenyl)-5-tert-butyl-1H-pyrazole-3-carboxylate and 2-chlorophenylboronic acid (0.279 g, 1.78 mmol) in n-propanol:water (2.35 ml:0.482 ml) mixture were added palladium acetate (0.005 g), triphenylphosphine (0.016 g) and 2N sodium carbonate (0.497 ml) and the solution was refluxed for 16 hours. To the reaction, a 2N solution of NaOH (1.5 ml) was added and refluxed for an additional 2 hours. The solution was cooled, acidified with 10% citric acid and extracted into ethyl acetate. The organic phase was washed with brine, dried over sodium sulfate, filtered and concentrated to give 0.212 g of 5-tert-butyl-1-(2′-chloro-1,1′-biphenyl-3-yl)-1H-pyrazole-3-carboxylic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07589116B2
出典データセットuspto-grants-2009_09
ORD IDord-3b54fcb58b5f418dbddf2a237380cde7
出典メモuspto-grants-2009_09