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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597431Generated: November 1, 2026

Potassium ethylxanthate → HCID 88234431, compound

https://huagongshe.com/reaction/1597431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium ethylxanthateHCID 2735045—
Reactant4-(4-(Trifluoromethoxy)phenoxy)anilineHCID 11666192—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductHCID 88234431HCID 88234431—

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-a8f7d583d7224fd2a082e6da510d371d
Source noteuspto-grants-2001_09