HRID1501190

反应详情

EQUATION

反应方程式

HRID 1501190 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of lithium diisopropylamide (2 mol/L, 22 mL, 44 mmol) in tetrahydrofuran (80 mL) was dropwise a solution of methyl 2-(4-bromophenyl)acetate (10 g, 44 mmol) in tetrahydrofuran (20 mL) at −78° C. The mixture solution was stirred for 0.5 hour at that temperature, then iodomethane (8 g, 56 mmol) was added. The mixture was stirred for 10 minutes at −78° C., then was removed from the cooling bath and stirred for 0.5 hour. The reaction was quenched with sat. ammonium chloride, then diluted with ethyl acetate, washed with water, The organic layer concentrated to dry, purified by column chromatography (silica-gel, petroleum:ethyl acetate=20:1) to give methyl 2-(4-bromophenyl)propanoate as a colorless oil (10 g, 91%). 1H NMR (300 MHz, CDCl3): δ 7.44 (d, J=9 Hz, 2H), 7.17 (d, J=9 Hz, 2H), 3.65-3.70 (m, 4H), 1.48 (d, J=6 Hz, 3H).

WORKUP

后处理

  1. customat −78° C
  2. stirringThe mixture was stirred for 10 minutes at −78° C.
  3. customwas removed from the cooling bath
  4. stirringstirred for 0.5 hour
  5. customThe reaction was quenched with sat. ammonium chloride
  6. additiondiluted with ethyl acetate
  7. washwashed with water
  8. concentrationThe organic layer concentrated
  9. customto dry
  10. custompurified by column chromatography (silica-gel, petroleum:ethyl acetate=20:1)