HRID481745

反应详情

EQUATION

反应方程式

HRID 481745 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

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.

WORKUP

后处理

  1. customwas degassed with a stream of nitrogen
  2. additionThe mixture was diluted with water (50 mL) and ethyl acetate (100 mL)
  3. dry with materialthe organic layer was dried over sodium sulfate
  4. concentrationconcentrated
  5. customaffording a yellow solid
  6. extractionthe resulting solution was extracted with ethyl acetate
  7. extractionagain was extracted with ethyl acetate
  8. dry with materialThe combined organic extracts were dried with sodium sulfate
  9. concentrationconcentrated to an oily solid, which
  10. customwas triturated with 2:1 hexane/ethylacetate