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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326042Generated: October 25, 2026

Quinoline → Ethyl 2-[4-(3-nitroquinolin-4-yloxy)phenoxy]propionate

https://huagongshe.com/reaction/326042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinolineHCID 7047—
ReactantPropanoic acid, 2-(4-hydroxyphenoxy)-, ethyl esterHCID 3017597—
Reactant4-Chloro-3-nitroquinolineHCID 11275808—
ProductEthyl 2-[4-(3-nitroquinolin-4-yloxy)phenoxy]propionateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04444584
Source datasetuspto-grants-1984_04
ORD IDord-d10dd75f0ecb40c78bfc1d34217c79f7
Source noteuspto-grants-1984_04