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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276090Generated: October 26, 2026

2-Aminothiazole → 1-(4-Chlorophenoxy)-2-nitrobenzene

https://huagongshe.com/reaction/2276090

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant4-ChlorophenolHCID 4684—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant2-(4-Chlorophenoxy)anilineHCID 76010—
Product1-(4-Chlorophenoxy)-2-nitrobenzeneHCID 301605071%
ProductN-[2-(4-Chlorophenoxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973278262%

Reaction Steps

2-(4-Chlorophenoxy)-1-nitrobenzene (0.88 g, 71%) was prepared from 4-chlorophenol (0.70 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(4-chlorophenoxy)aniline (0.50 g, 65%) following general procedure B. N-[2-(4-Chlorophenoxy)phenyl]-N′-(thiazol-2-yl)urea (106 mg, 62%) was prepared from 2-(4-chlorophenoxy)aniline (109 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045670E1
Source datasetuspto-grants-2015_09
ORD IDord-b4403725e84e48be930526e3b786de3f
Source noteuspto-grants-2015_09