HRID518166

反应详情

EQUATION

反应方程式

HRID 518166 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

NaOH (160 mg, 4 mmol) in H2O (2 ml) was added to a suspension of (E)-3-{1′-tert-butoxycarbonyl-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid methyl ester (462 mg, 1.15 mmol, Intermediate 1, Step B) in MeOH (6 ml). The mixture was stirred at 50° C. After 2 h, MeOH was evaporated and the pH of the aqueous phase was adjusted with 1 M HCl to a pH value of 5. The resulting suspension was extracted with DCM, the organic phase dried over Na2SO4 and concentrated to give (E)-3-{1′-tert-butoxycarbonyl-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid (410 mg) as a white solid.

WORKUP

后处理

  1. customMeOH was evaporated
  2. extractionThe resulting suspension was extracted with DCM
  3. dry with materialthe organic phase dried over Na2SO4
  4. concentrationconcentrated