HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → Ethyl 2-[4-(2-bromoquinolin-4-yloxy)phenoxy]propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | 2-Bromo-4-nitroquinoline | HCID 581266 | — |
| Reactant | Propanoic acid, 2-(4-hydroxyphenoxy)-, ethyl ester | HCID 3017597 | — |
| Product | Ethyl 2-[4-(2-bromoquinolin-4-yloxy)phenoxy]propionate | HCID 20461964 | — |
Reaction Steps
Ethyl 2-[4-(2-bromoquinolin-4-yloxy)phenoxy]propionate (40) was prepared from 2-bromo-4-nitroquinoline (Chem Abstracts 51: 6639) and ethyl 2-(4-hydroxyphenoxy)-propionate following essentially the same procedure as that described in Example 1. The compound was isolated as a colourless oil which solidified slowly on standing. Proton magnetic resonance spectrum (CDCl3 ; δ in ppm): 8.5-7.4 (4H, m, quinoline protons); 7.1 (4H, d of d, phenyl protons); 6.6 (1H, s, C3 quinoline proton); 4.8 (1H, q, CHCH3); 4.3 (2H, q, OCH2CH3); 1.65 (3H, d, CHCH3); 1.3 (3H t, OCH2CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04444584 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-f2a6132572cd470096f96f4457c7b91f |
| Source note | uspto-grants-1984_04 |