HRID1443712

反应详情

EQUATION

反应方程式

HRID 1443712 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Add boron tribromide (39 mL, 39 mmol, 1.0 M solution in CH2Cl2) dropwise to a stirred −78° C. solution of 5-[5-(5-chloro-2-methoxy-phenyl)-isoxazol-3-yl]-pentanoic acid ethyl ester (4.39 g, 13 mmol) in CH2Cl2 (40 mL). Allow to warm to room temperature. After 2 hours, cool to −78° C. and add boron tribromide (13 mL, 13 mmol, 1.0 M solution in CH2Cl2) dropwise and allow to warm to room temperature overnight. Quench via dropwise addition of ethanol (60 mL, absolute). Concentrate, dissolve residue in CHCl3, wash with saturated NaHCO3 solution (×2), dry over MgSO4 and concentrate to get 3.7 g of a tan solid. Adsorb on SiO2 and purify the residue by flash chromatography on silica gel eluting with 0-60% EtOAc/hexanes to afford the title compound (3.3 g, 78%). MS (IS) 324 (M+1)+.

WORKUP

后处理

  1. temperaturecool to −78° C.
  2. temperatureto warm to room temperature overnight
  3. customQuench via dropwise addition of ethanol (60 mL, absolute)
  4. concentrationConcentrate
  5. dissolutiondissolve residue in CHCl3
  6. washwash with saturated NaHCO3 solution (×2)
  7. dry with materialdry over MgSO4
  8. concentrationconcentrate