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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1470137생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1470137

반응식

참여 물질

역할이름HCID투입량
반응물Phosphoric AcidHCID 1004—
반응물Triisopropyl borateHCID 21531—
반응물tert-Butyl 4-(3-bromophenyl)piperazine-1-carboxylateHCID 10882380—
반응물ButyllithiumHCID 178418339—
용매Tetrahydrofuran tolueneHCID 22635083—
생성물(3-[4-(Tert-butoxycarbonyl)piperazin-1-YL]phenyl)boronic acidHCID 22392008—

반응 조건

온도-70 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09006281B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-c3c7229611774d5cbb7b3126e6e349d3
출처 메모uspto-grants-2015_04