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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597430Generated: October 31, 2026

p-Fluoronitrobenzene → 4-[4-(trifluoromethoxy)phenoxy]aniline

https://huagongshe.com/reaction/1597430

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
Reactantp-(Trifluoromethoxy)phenolHCID 70015—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Product4-[4-(trifluoromethoxy)phenoxy]anilineHCID 11666192—

Reaction Steps

Reaction of 4-fluoro-nitrobenzene with 4-trifluoromethoxyphenol in the presence of KOtBu as described in Example 74A, followed by reduction of the nitro group (hydrogen, 10% Pd/C) gave 4-(4-trifluoromethoxyphenoxy)-aniline. The aniline (4.58 g, 17 mmol) was dissolved in conc. HCl (3.1 mL) and ice (4.5 g) cooled to −5 C., then treated with a solution of NaNO2 (1.17 g, 17 mmol) in water (7mL) which was added dropwise. The cold soltion was added to an aqueous (7 mL) solution of potassium xanthate (5.46 g, 34 mmol) and the resulting mixture was heated at 70 C for 2 h, then allowed to cool to rt and partitioned between EtOAc and water. The organic extract was dried (MgSO4), filt ered and concentrated to give the title compound

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294573B1
Source datasetuspto-grants-2001_09
ORD IDord-187d79ebbc23405bb705c12980ff043b
Source noteuspto-grants-2001_09