反应 #816386

ord-7edc6e62b38842c4962ead419202b6d3

反应方程式

[C-]#N.[K+]
KCN
O=C(Cl)c1ccccc1
benzoyl chloride
ClCCl.O
water methylene chloride
c1ccc2c(c1)ccc1ncccc12
benzo(f)chinolin
N#CC1C=Cc2c(ccc3ccccc23)N1C(=O)c1ccccc1
3-cyano-4-benzoyl-3,4-dihydrobenzo(f)chinoline

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The organic phase was separated
  2. 2
    洗涤washed with water, 5% hydrochloric acid, water, 5% NaOH solution
  3. 3
    干燥After drying over magnesium sulfate
  4. 4
    其他the solution was evaporated to dryness

实验过程

648 μl (5.58 mmol) benzoyl chloride was added to a two phase system of water/methylene chloride over a period of two hours. These two layers contain 500 mg (2.79 mmol) of benzo(f)chinolin in the methylene chloride layer and 545 mg (8.37 mmol) KCN in water. Stirring was continued for 6 hours. The organic phase was separated and washed with water, 5% hydrochloric acid, water, 5% NaOH solution, and again with water. After drying over magnesium sulfate, the solution was evaporated to dryness.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07582295B2uspto-grants-2009_09