反应 #2139932

ord-7d2196d0a09441f3bd870125976e9caa

反应方程式

c1ccc2c(c1)Nc1ccccc1S2
phenothiazine
CCI
iodoethane
[K+].[OH-]
potassium hydroxide
CCN1c2ccccc2Sc2ccccc21
10-Ethylphenothiazine

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度was refluxed for 24 hours
  2. 2
    温度After cooling
  3. 3
    过滤the reaction mixture was filtered
  4. 4
    其他the solvent was evaporated
  5. 5
    其他The product was crystallized from methanol
  6. 6
    其他was 103-104° C

实验过程

A mixture of 10 g (0.05 mol) of phenothiazine (obtained from Fluka), 11.7 g (0.075 mol) of iodoethane (obtained from Aldrich), 4.2 g (0.075 mol) of potassium hydroxide, and 0.25 g of tetra-n-butylammonium hydrogen sulfate (obtained from Aldrich) in 200 ml of dry toluene was refluxed for 24 hours. After cooling, the reaction mixture was filtered, and the solvent was evaporated. The product was crystallized from methanol. The yield of 10-ethylphenothiazine was 10.2 g (90%). The melting point of the product was 103-104° C. The 1H-NMR spectrum (100 MHz) of the product in CDCl3 was characterized by the following chemical shifts (δ, ppm): 1.40 (t, J=7.0 Hz, 3H, CH3); 3.90 (q, J=7.0 Hz, 2H, CH2); 6.78-7.32 (m, 8H, Ar).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07326506B2uspto-grants-2008_02