HRID1825157

反应详情

EQUATION

反应方程式

HRID 1825157 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-20 °C

PROCEDURE

实验过程

To a solution of (5-methoxy-2-methyl-phenyl)-carbamic acid t-butyl ester (6.95 g, 29.3 mmole) in 100 ml THF cooled at −45° C. was added sec-BuLi (45 ml, 58.5 mmole) slowly to keep temperatue lower than −45° C. The reaction mixture was stirred and warmed to −20° C., then cooled to −45° C. and propionaldehyde (2.67 ml, 36.63 mmole) was added. The reaction mixture was stirred and warmed to room temperature for 1 h, quenched with 1N HCl and extracted with EtOAc, dried over MgSO4 and concentrated. The residue was purified by flash column chromatography (10–15% EtOAc in hexane) to give colorless oil (3.40 g, 39%). 1H NMR (CDCl3) δ 7.96 (1H, s), 7.44 (1H, s), 6.96–7.00 (1H, m), 6.55 (1H, m), 3.80 (3H, s), 2.60–2.76 (2H, m), 1.93–1.95 (2H, m), 1.50 (9H, s), 0.93–1.01 (4H, m). ESIMS (MNa+): 318.20.

WORKUP

后处理

  1. customlower than −45° C
  2. temperaturecooled to −45° C.
  3. stirringThe reaction mixture was stirred
  4. temperaturewarmed to room temperature for 1 h
  5. customquenched with 1N HCl
  6. extractionextracted with EtOAc
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated
  9. customThe residue was purified by flash column chromatography (10–15% EtOAc in hexane)