反应详情

温度

22 °C

3-Acetamido-5-amino-2,4,6-triiodobenzoic acid (I; 228.76 g., 0.4 mole) was added to an anhydrous ethanolic solution of sodium ethoxide (prepared from 18.4 g. (0.8 g. atom) of sodium) at 45° C. After 10 minutes, the homogeneous solution was cooled to 22° C. and methyl iodide (62.48 g.; 0.44 mole) was added. The reaction mixture was heated at 50°-55° C. for 30 minutes, at 62° C. for 30 minutes and finally at 68°-70° C. for 15 minutes. The reaction mixture was now pH 8. Methyl iodide (1 ml.) was added and heating was continued at 70° C. for 15 minutes after which the solution was neutral. The ethanol was removed under reduced pressure and water (1300 ml.) was added to the residue. The solid which dropped out of solution was collected; the filtrate was basified (~pH 10) with 50% sodium hydroxide and was washed with a 3:1 chloroform-isopropyl alcohol mixture (800 ml.). The aqueous layer was acidified to pH 5 with acetic acid and treated with activated charcoal marketed under the trade designation "Darco G-60" (5 g.) for 1 hour. The filtered solution was added to 6 N hydrochloric acid (700 ml.) at room temperature to precipitate the product. The precipitate was digested for 10 minutes and was then collected, washed with water (500 ml.), and dried at 60° C. overnight to yield 193.5 g. of 3-amino-2,4,6-triiodo-5-(N-methylacetamido)benzoic acid (82.6% yield). The product was homogeneous by thin-layer chromatography (chloroform-ethyl acetateacetic acid, 30:20:1) and the structure of the product was confirmed by nuclear magnetic resonance spectroscopy.

1. temperatureThe reaction mixture was heated at 50°-55° C. for 30 minutes, at 62° C. for 30 minutes and finally at 68°-70° C. for 15 minutes
2. temperatureheating
3. waitwas continued at 70° C. for 15 minutes
4. customThe ethanol was removed under reduced pressure and water (1300 ml.)
5. additionwas added to the residue
6. additionThe solid which dropped out of solution
7. customwas collected
8. washwas washed with a 3:1 chloroform-isopropyl alcohol mixture (800 ml.)
9. additiontreated with activated charcoal
10. wait" (5 g.) for 1 hour
11. additionThe filtered solution was added to 6 N hydrochloric acid (700 ml.) at room temperature
12. customto precipitate the product
13. waitThe precipitate was digested for 10 minutes
14. customwas then collected
15. washwashed with water (500 ml.)
16. customdried at 60° C. overnight
17. customto yield 193.5 g