HRID1339

反应详情

EQUATION

反应方程式

HRID 1339 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A 3.32 g portion of 2,3,4,5-tetrahydro-1H-1-benzazepin-5-one and 4.31 ml of triethylamine were dissolved in 33 ml of dichloromethane and, with stirring on an ice bath, 4.59 g of p-nitrobenzoyl chloride was added to the resulting solution. The reaction solution was stirred at room temperature for additional 60 minutes. The reaction solution was then mixed with a saturated sodium bicarbonate aqueous solution and subjected to phase separation. The dichloromethane layer was separated and washed with a 1N hydrochloric acid aqueous solution and a saturated sodium chloride aqueous solution once for each. The thus washed layer was dried over anhydrous magnesium sulfate and then concentrated under a reduced pressure. The thus obtained residue was recrystallized from methyl alcohol to obtain 5.68 g of 1-(4-nitrobenzoyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one.

WORKUP

后处理

  1. stirringThe reaction solution was stirred at room temperature for additional 60 minutes
  2. customsubjected to phase separation
  3. customThe dichloromethane layer was separated
  4. washwashed with a 1N hydrochloric acid aqueous solution
  5. dry with materialThe thus washed layer was dried over anhydrous magnesium sulfate
  6. concentrationconcentrated under a reduced pressure
  7. customThe thus obtained residue was recrystallized from methyl alcohol