HRID1822958

反应详情

EQUATION

反应方程式

HRID 1822958 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
35 °C

PROCEDURE

实验过程

To a solution of 7-fluoro-4-methoxy-1-benzothiophen-2(3H)-one (1.06, 5.4 mmol) in dichloromethane (10 mL) at 0° C. was added slowly a solution of diisobutylaluminium hydride in dichloromethane (1 M, 8.04 mL, 8.0 mmol). After 30 mins the reaction was quenched by careful addition of aqueous hydrochloric acid (6 N, 25 mL). The mixture was concentrated to remove the dichloromethane, the aqueous residue was then stirred at 35° C. for 2 h. The aqueous solution was extracted with diethyl ether (3×50 mL), washed with aqueous sodium hydroxide (2 N, 50 mL), brine (50 mL) then dried (MgSO4) and the solvent evaporated in vacuo to give the title compound (0.86 g, 87%) as a purple oil; δH 7.44–7.38 (1H, m, ArH), 7.36–7.24 (1H, m, ArH), 6.88–6.80 (1H, m, ArH), 6.57–6.49 (1H, m, ArH) and 3.82 (3H, s, OCH3).

WORKUP

后处理

  1. customAfter 30 mins the reaction was quenched by careful addition of aqueous hydrochloric acid (6 N, 25 mL)
  2. concentrationThe mixture was concentrated
  3. customto remove the dichloromethane
  4. extractionThe aqueous solution was extracted with diethyl ether (3×50 mL)
  5. washwashed with aqueous sodium hydroxide (2 N, 50 mL), brine (50 mL)
  6. dry with materialthen dried (MgSO4)
  7. customthe solvent evaporated in vacuo