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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278168Generated: November 4, 2026

2-(2-chloro-4-nitrophenoxy)naphthalene → 3-chloro-4-(2-naphthyloxy)aniline

https://huagongshe.com/reaction/1278168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-chloro-4-nitrophenoxy)naphthaleneHCID 921588—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
Product3-chloro-4-(2-naphthyloxy)anilineHCID 345128060.1%

Reaction Steps

3-Chloro-4-(2-naphthyloxy)nitrobenzene (14.8 g) and platinum dioxide (0.1 g) were suspended in a mixture of benzene and ethanol (1:1) (200 ml), and hydrogenation was carried out until 3.2 liters of hydrogen were absorbed. After removal of the solvent from the reaction mixture by distillation under reduced pressure, the residue was distilled in vacuo to give 3-chloro-4-(2-naphthyloxy)aniline (8 g) as a fraction boiling at 173° to 198° C./0.2 to 0.3 mmHg. M.P., 67°-69° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04280835
Source datasetuspto-grants-1981_07
ORD IDord-efc47d8e54434ed28e9794fd7e8a14ce
Source noteuspto-grants-1981_07