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HRID 38116作成日:2026年10月26日

Water → Tert-butyl(trans)-2-(1,1'-biphenyl-4-yl)cyclopropylcarbamate

https://huagongshe.com/reaction/38116

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物Boronic AcidHCID 61668—
反応物tert-butyl ((1R,2S)-2-(4-bromophenyl)cyclopropyl)carbamateHCID 86658779—
触媒HCID 178418397HCID 178418397—
溶媒Acetonitrile--water (1/1)HCID 18373917—
生成物Tert-butyl(trans)-2-(1,1'-biphenyl-4-yl)cyclopropylcarbamateHCID 86658778—

反応手順

A solution of tert-butyl(trans)-2-(4-bromophenyl)cyclopropylcarbamate (Intermediate F; 1 equiv), 1.2 equiv of the boronic acid, 3.0 equiv of K2CO3 in CH3CN+H2O (4:1) was degassed for 30 mins with Argon gas, added 0.01 equiv of Pd (PPh3)4, heated the reaction mixture at reflux temp for 4 h. The progress of the reaction was monitored by TLC, after completion, poured the reaction mixture into water, extracted with EtOAc. The combined extracts were washed with water, brine, dried over anhydrous Na2SO4, filtered and evaporated. The crude residue was purified by column chromatography to get tert-butyl(trans)-2-(1,1′-biphenyl-4-yl)cyclopropylcarbamate derivative

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524717B2
出典データセットuspto-grants-2013_09
ORD IDord-40bdd2650dc84da68d73597eb7e292c0
出典メモuspto-grants-2013_09