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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637987Generated: October 30, 2026

Hydrochloric Acid → 4-{[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}aniline

https://huagongshe.com/reaction/637987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsopropanolHCID 3776—
Reactant2-(4-Nitrophenoxy)-3-chloro-5-trifluoromethyl pyridineHCID 2775736—
CatalystIronHCID 23925—
SolventWaterHCID 962—
Product4-{[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}anilineHCID 276411680.6%

Reaction Steps

A mixture of 3-chloro-5-trifluoromethyl-2-(4-nitrophenoxy)pyridine (1.0 g), iron powder (3.2 g), isopropyl alcohol (60 ml), water (6 ml) and dilute hydrochloric acid (0.2 ml of a 2N solution), were heated at the reflux temperature for 12 hours. After cooling and filtering to remove the solid matter, the filtrate was concentrated by evaporation of the volatile portion under reduced pressure. The residual solid was recrystallised from n-hexane to yield 2-(4-aminophenoxy)-3-chloro-5-trifluoromethylpyridine (0.73 g) m.p. 85°-87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04559353
Source datasetuspto-grants-1985_12
ORD IDord-955ff5a690e846b3a309b3bf2db62aad
Source noteuspto-grants-1985_12