HRID37662

反应详情

EQUATION

反应方程式

HRID 37662 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

(R)-3-(N-Isopropyl, N-n-propylamino)-5-trifluoromethanesulfonyloxychroman (1 g, 2.6 mmol) was dissolved in toluene (25 mL) under a nitrogen atmosphere. Ethanol (11.5 mL), LiCl (0.22 g, 5.2 mmol), Na2CO3 (2M, 3.8 mL), Pd(PPh3)4 (0.054 g, 0.047 mmol) and phenylboronic acid (0.38 g, 3.1 mmol) were added and the reaction mixture was stirred at 90° C. for 7 h. The solvent removed in vacuo until 15 mL was left. The residue was diluted with diethyl ether, washed with NH3 (2M) twice and dried (MgSO4). Removal of the solvent in vacuo gave a yellow-brownish oily residue which was purified by flash chromatography )SiO2, CH2Cl2) to give the title compound in 86% yield (0.7 g). α=-50.7° (MeOH, 0.1M, 22° C.). The HCl-salt was precipitated from ether by the slow addition of HCl in ether to an ice-cold solution of the base. The crude salt was recrystallized from EtOAc/diethyl ether to give 650 mg of needle-like crystals. Mp. 141°-142° C.

WORKUP

后处理

  1. customThe solvent removed in vacuo until 15 mL
  2. waitwas left
  3. additionThe residue was diluted with diethyl ether
  4. washwashed with NH3 (2M) twice
  5. dry with materialdried (MgSO4)
  6. customRemoval of the solvent in vacuo
  7. customgave a yellow-brownish oily residue which
  8. customwas purified by flash chromatography )SiO2, CH2Cl2)