反应 #1597015

ord-f7371c5d6ddf4995b96f3264db1f0942

反应方程式

O=C(O)c1ccccc1O
salicylic acid
Nc1ccc([N+](=O)[O-])cc1Cl
2-chloro-4-nitroaniline
ClP(Cl)Cl
phosphorous trichloride
ClCCl
dichloromethane
O=C(Nc1ccc([N+](=O)[O-])cc1Cl)c1ccccc1O
title compound
O=C(Nc1ccc([N+](=O)[O-])cc1Cl)c1ccccc1O
N-(2-chloro-4-nitrophenyl)-2 hydroxybenzamide

反应条件

温度
137°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The solution was cooled to about 125° C
  2. 2
    温度to cool to room temperature
  3. 3
    其他The product separated
  4. 4
    过滤was collected by filtration
  5. 5
    洗涤washed with hexanes
  6. 6
    其他recrystallized from ethanol

实验过程

The method disclosed in U.S. Pat. No. 3,079,297 to Shraufstatter et al with minor variations was utilized. A boiling solution of salicylic acid (1.03 g, 7.46 mmol) and 2-chloro-4-nitroaniline (1.29 g, 7.46 mmol) in xylenes (20 mL) was treated dropwise with a solution of phosphorous trichloride in dichloromethane 2.0M, 1.50 mL, 0.40 equiv.), and the resulting solution was refluxed (137° C.) for four hours. The solution was cooled to about 125° C. An oily residue covered the bottom and sides of the reaction vessel. The hot reaction solution was transferred by glass pipette to a beaker and was allowed to cool to room temperature while being stirred rapidly. The product separated, was collected by filtration, and washed with hexanes, then recrystallized from ethanol. The title compound was obtained, MP 218-220° C. (dec.). 1HNMR (500 MHz, DMSO-d6): δ 7.02 (m, 1H, H3), 7.07 (m, 1H, H5), 7.49 (m, 1H, H4), 8.04 (m, 1H, H6), 8.28 (m, 1H, H5′), 8.41 (m, 1H, H3′), 8.85 (m, 1H, H6′), 11.8 (s, 1H, NH), 12.34 (s, 1H, OH).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08211882B2uspto-grants-2012_07