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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81494생성일: 2026년 10월 26일

Hydrochloric Acid → [5-(Trifluoromethyl)pyridin-3-yl]boronic acid

https://huagongshe.com/reaction/81494

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Triethyl borateHCID 9009—
반응물3-Bromo-5-(trifluoromethyl)pyridineHCID 11127991—
반응물Isohexane ethyl acetateHCID 21882781—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물[5-(Trifluoromethyl)pyridin-3-yl]boronic acidHCID 45158900—

반응 조건

온도-78 °C

반응 단계

Triethylborate (24 ml, 139 mmol) is added to a solution of 3-bromo-5-trifluoromethyl-pyridine (30 g, 133 mmol) in THF (300 ml) and the resulting pale yellow solution is cooled to −78° C. A solution of 1.6 M n-butyl lithium in hexanes (97 ml, 139 mmol) is added via cannula dropwise over 40 minutes, keeping the temperature below −65° C. Once addition is complete, the reaction mixture is allowed to warm slowly to room temperature and stirred for 1 hour. 1M HCl (200 ml) is added and the reaction mixture stirred for 15 minutes. The layers are separated and the organic layer is washed with 1M HCl (200 ml). The aqueous layers are combined and washed with EtOAc (2×250 ml). The pH of the aqueous phase is adjusted by the addition of 2M NaOH, and extracted with EtOAc (2×250 ml). Concentration in vacuo affords a solid, which is recyrstallised from EtOAc/iso-hexane to yield the title compound as a yellow solid [M+H]+ 192.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846687B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-50ae31e39c944dd8a487edfe853fb192
출처 메모uspto-grants-2014_09