HRID37669

反应详情

EQUATION

反应方程式

HRID 37669 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
70 °C

PROCEDURE

实验过程

(R)-8-Fluoro-3-(N,N-di-n-propylamino)-5-trifloromethanesulfonyloxychroman (0.95 g, 2.4 mmol), triethylamine (0.53 g, 5.2 mmol), 1,3bis-(diphenylphosphino)propane (100 mg, catalytic amount), palladium(II)acetate (50 mg, catalytic amount) and DMF/MeOH (18 mL, 6:2) were mixed in a 50 mL three necked round bottom flask. The flask was evacuated followed by the inlet of CO (repeated three times). The reaction mixture was stirred at 70° C. for 7 hours. The solvent was removed in vacuo and the residue was dissolved in diethyl ether/2M NH3. The layers were separated and the water phase was extracted once with ether. The combined ether layers were dried (MgSO4) and the solvent was removed in vacuo to give a brown oily residue which was purified by flash chromatography (SiO2, CH2Cl2 /EtOAC, 20:1) to give 650 mg of the title compound as a clear oil (87% yield). [α]21 -92° (c 10 mg/mL MeOH). Mass spectrum (70 eV) m/z (relative intensity) 309(20, M+), 281(18), 280(100), 56(10), 43(22), 42(12), 41(16).

WORKUP

后处理

  1. customThe flask was evacuated
  2. customThe solvent was removed in vacuo
  3. dissolutionthe residue was dissolved in diethyl ether/2M NH3
  4. customThe layers were separated
  5. extractionthe water phase was extracted once with ether
  6. dry with materialThe combined ether layers were dried (MgSO4)
  7. customthe solvent was removed in vacuo
  8. customto give a brown oily residue which
  9. customwas purified by flash chromatography (SiO2, CH2Cl2 /EtOAC, 20:1)