HRID357309

反应详情

EQUATION

反应方程式

HRID 357309 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
55 °C

PROCEDURE

实验过程

A suspension of (S)-3-(2-amino-3-nitrophenoxy)-1,2-epoxypropane (5 g, 23.8 mmol) and 4-(4-(2-amino-2-methylpropyl)phenoxy)benzamide (20.3 g 71.1 mmol) in absolute ethanol (200 mL) was heated to 55° C. for 12 h. All solids went into solution at 50° C. Upon completion of the reaction, the solvent was evaporated to dryness. The residue was redissolved in ethyl acetate and washed with a saturated solution of sodium bicarbonate. The layers were separated and the aqueous phase was extracted with ethyl acetate. The two organic layers were combined and washed with brine. The phases were separated and the organic layer was dried over sodium sulfate, filtered, and the solvent evaporated. column chromatography eluting with 20% MeOH/CHCl3 gave 7.26 g (62%) of product. NMR. MS.

WORKUP

后处理

  1. customwent into solution at 50° C
  2. customUpon completion of the reaction
  3. customthe solvent was evaporated to dryness
  4. dissolutionThe residue was redissolved in ethyl acetate
  5. washwashed with a saturated solution of sodium bicarbonate
  6. customThe layers were separated
  7. extractionthe aqueous phase was extracted with ethyl acetate
  8. washwashed with brine
  9. customThe phases were separated
  10. dry with materialthe organic layer was dried over sodium sulfate
  11. filtrationfiltered
  12. customthe solvent evaporated
  13. washcolumn chromatography eluting with 20% MeOH/CHCl3