HRID1430475

反应详情

EQUATION

反应方程式

HRID 1430475 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
55 °C

PROCEDURE

实验过程

A solution of ethyl 2-(2-bromo-4-fluoro-5-nitrophenyl)acetate (2.127 g, 6.95 mmol) in EtOH (70 mL) was treated with iron powder (3.88 g, 69.5 mmol) and satd ammonium chloride (14.48 mL, 69.5 mmol) and heated to 55° C. for 1 h. The mixture was cooled to RT, filtered through a pad of diatomaceous earth, rinsed well with EtOH and the organics concentrated under reduced pressure. The resulting aqueous residue was treated with satd. NaHCO3, extracted with EtOAc (2×) and the combined organics were washed with water, dried (MgSO4), and concentrated to afford ethyl 2-(5-amino-2-bromo-4-fluorophenyl)acetate (1.792 g, 93% yield) as an amber oil. 1H NMR (400 MHz, DMSO-d6): δ 7.25 (d, 1H), 6.76 (d, 1H), 5.35 (s, 2H), 4.08 (q, 2H), 3.61 (s, 2H), 1.18 (t, 3H); MS (ESI) m/z: 278.0 [M+H]+.

WORKUP

后处理

  1. temperatureThe mixture was cooled to RT
  2. filtrationfiltered through a pad of diatomaceous earth
  3. washrinsed well with EtOH
  4. concentrationthe organics concentrated under reduced pressure
  5. additionThe resulting aqueous residue was treated with satd
  6. extractionNaHCO3, extracted with EtOAc (2×)
  7. washthe combined organics were washed with water
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated