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HRID 81494作成日:2026年10月26日

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

https://huagongshe.com/reaction/81494

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Triethyl borateHCID 9009—
反応物3-Bromo-5-(trifluoromethyl)pyridineHCID 11127991—
反応物Isohexane ethyl acetateHCID 21882781—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物[5-(Trifluoromethyl)pyridin-3-yl]boronic acidHCID 45158900—

反応条件

温度-78 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846687B2
出典データセットuspto-grants-2014_09
ORD IDord-50ae31e39c944dd8a487edfe853fb192
出典メモuspto-grants-2014_09