反应 #6674

ord-aab5b1b567764967a3b9eb9b16000b36

反应方程式

[K+].[OH-]
potassium hydroxide
O=P(Cl)(Cl)Cl
Phosphorus oxychloride
CN(C)C=O
dimethylformamide
CCN1c2ccccc2Sc2ccccc21
10-ethylphenothiazine
CN(C)C=O
DMF
CCN1c2ccccc2Sc2cc(C=O)ccc21
10-Ethylphenothiazine-3-carbaldehyde

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The reaction mixture was refluxed at 80° C. for 24 hours
  2. 2
    萃取The product was extracted with chloroform
  3. 3
    萃取The chloroform extract
  4. 4
    干燥was dried with anhydrous sodium sulfate
  5. 5
    过滤filtered
  6. 6
    workup.DISTILLATIONdistilled
  7. 7
    其他The product was crystallized from methanol

实验过程

Phosphorus oxychloride (POCl3,3.7 ml, 0.04 mol) was added dropwise to 4.4 ml (0.06 mol) of dry dimethylformamide (DMF) at 0° C. under a nitrogen atmosphere. This solution was warmed up slowly to room temperature. Then, a solution of 5 g (0.02 mol) of 10-ethylphenothiazine in dry DMF was added dropwise. The reaction mixture was refluxed at 80° C. for 24 hours and poured into the ice water. This solution was neutralized with potassium hydroxide until the pH reached 6–8. The product was extracted with chloroform. The chloroform extract was dried with anhydrous sodium sulfate, filtered and distilled. The product was crystallized from methanol. The yield of 10-ethylphenothiazine-3-carbaldehyde (C15H13NOS, FW=255.34) was 65%.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07083884B2uspto-grants-2006_08