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HRID 1470137作成日:2026年10月25日

Phosphoric Acid → (3-[4-(Tert-butoxycarbonyl)piperazin-1-YL]phenyl)boronic acid

https://huagongshe.com/reaction/1470137

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphoric AcidHCID 1004—
反応物Triisopropyl borateHCID 21531—
反応物tert-Butyl 4-(3-bromophenyl)piperazine-1-carboxylateHCID 10882380—
反応物ButyllithiumHCID 178418339—
溶媒Tetrahydrofuran tolueneHCID 22635083—
生成物(3-[4-(Tert-butoxycarbonyl)piperazin-1-YL]phenyl)boronic acidHCID 22392008—

反応条件

温度-70 °C

反応手順

Into a 250-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of tert-butyl 4-(3-bromophenyl)piperazine-1-carboxylate (3.8 g, 11.14 mmol, 1.00 equiv) in toluene/tetrahydrofuran=1:1 (40 mL). This was followed by the addition of n-BuLi (4.9 mL, 2.5M/L) dropwise with stirring at −70° C. The resulting solution was stirred for 30 min at −70° C. To this was added triisopropyl borate (2.5 g, 13.30 mmol, 1.19 equiv) dropwise with stirring at −70° C. The mixture was warmed to 0° C., the reaction was then quenched by the addition of 13 mL of saturated ammonium chloride and 3.4 mL of water. Phosphoric acid (85 wt %, 1.5 g, 1.2 equiv) was added and the mixture was stirred for 30 min. The organic layer was separated and dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was dissolved in 20 mL of toluene. The product was precipitated by the addition of 80 mL of heptane. The solids were washed with 20 mL of heptane and collected by filtration. This resulted in 2.9 g (85%) of 3-(4-(tert-butoxycarbonyl)piperazin-1-yl)phenylboronic acid as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09006281B2
出典データセットuspto-grants-2015_04
ORD IDord-c3c7229611774d5cbb7b3126e6e349d3
出典メモuspto-grants-2015_04