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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 481745생성일: 2026년 10월 25일

Hydrochloric Acid → 2-Phenyl-3-pyridinol

https://huagongshe.com/reaction/481745

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-Bromo-3-pyridinolHCID 23070—
반응물Phenylboronic AcidHCID 66827—
용매EthanolHCID 702—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Sodium HydroxideHCID 14798—
생성물2-Phenyl-3-pyridinolHCID 1870545.4%

반응 조건

온도100 °C

반응 단계

A mixture of 2-bromo-3-hydroxypyridine (2.20 g, 12.6 mmol), phenylboronic acid (2.00 g, 16.3 mmol) and palladium (tetrakis)triphenylphosphine (250 mg) in toluene (30 mL), ethanol (15 mL) and 5% aqueous sodium hydroxide (15 mL) was degassed with a stream of nitrogen and stirred vigorously at 100° C. overnight. The mixture was diluted with water (50 mL) and ethyl acetate (100 mL), and the organic layer was dried over sodium sulfate and concentrated, affording a yellow solid. This material was suspended in water (100 mL), a few mL of 1N HCl was added, and the resulting solution was extracted with ethyl acetate. The aqeuous layer was neutralized with saturated aqueous sodium bicarbonate, and again was extracted with ethyl acetate. The combined organic extracts were dried with sodium sulfate and concentrated to an oily solid, which was triturated with 2:1 hexane/ethylacetate, affording 0.98 g of 3-hydroxy-2-phenylpyridine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05789584
출처 데이터셋uspto-grants-1998_08
ORD IDord-8a5361bd9518460199bb79193a1b9d7c
출처 메모uspto-grants-1998_08