HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1-(3-Chlorophenyl)ethanone → 1-(5-Chloro-2-nitrophenyl)ethanone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1-(3-Chlorophenyl)ethanone | HCID 14933 | — |
| Edukt | Sulfuric acid, mixt. with nitric acid | HCID 71777668 | — |
| Produkt | 1-(5-Chloro-2-nitrophenyl)ethanone | HCID 255582 | — |
Reaktionsschritte
The intermediates, 5-alkylamino-2-aminoacetophenones (60-62) were prepared according to the methods reported before. As shown in Scheme 6, the starting 3-chloroacetophenone (54) was first nitrated with HNO3/H2SO4 to form the 5-chloro-2-nitroacetophenone (55) and 5-chloro-4-nitroacetophenone (56). Compound 55 was reacted separately with various alkylamines to yield the corresponding 5-alkylamino-2-nitroacetophenones (57-59). Catalytic hydrogenation of compounds 57-59 yielded the corresponding 5-alkylamino-2-aminoacetophenones (60-62). L. Ll, K. K. Wang, S. C. Kuo, T. S. Wu, D. Lednicer, C. M. Lin, E. Hamel and K. H. Lee, J. Med. Chem., 37, 1126-35. (1994), which is herein incorporated by reference in its entirety.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08524740B2 |
| Quelldatensatz | uspto-grants-2013_09 |
| ORD ID | ord-527955b53a8541d58d978baa492d3dfb |
| Quellennotiz | uspto-grants-2013_09 |