HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → Ethyl 2-[4-(3-nitroquinolin-4-yloxy)phenoxy]propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | Propanoic acid, 2-(4-hydroxyphenoxy)-, ethyl ester | HCID 3017597 | — |
| Reactant | 4-Chloro-3-nitroquinoline | HCID 11275808 | — |
| Product | Ethyl 2-[4-(3-nitroquinolin-4-yloxy)phenoxy]propionate | HCID 20461943 | — |
Reaction Steps
Ethyl 2-[4-(3-nitroquinolin-4-yloxy)phenoxy]propionate (41) was prepared from 4-chloro-3-nitroquinoline and ethyl 2-(4-hydroxyphenoxy)propionate following essentially the same procedure as that described in Example 1. The compound was isolated as a yellow oil. Proton magnetic resonance spectrum (CDCl3 ; δ in ppm): 9.3 (1H, s); 8.3-7.4 (4H, m, quinoline protons); 6.8 (4H, s, phenoxy protons); 4.7 (1H, q, CH--CH3); 4.2 (2H, q, OCH2 --CH3); 1.6 (3H, d, CH--CH3); 1.2 (3H, t, OCH2 --CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04444584 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-d10dd75f0ecb40c78bfc1d34217c79f7 |
| Source note | uspto-grants-1984_04 |