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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432917Generated: October 26, 2026

4-Fluorobenzenesulfonyl chloride → 5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-(4-fluoro-benzenesulfonyl)-benzene

https://huagongshe.com/reaction/432917

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
Reactant1,3-Dichloro-2-(4-methoxyphenoxy)-5-nitrobenzeneHCID 9972902—
SolventPhosphorus Pentoxide-Methanesulfonic AcidHCID 86584057—
Product5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-(4-fluoro-benzenesulfonyl)-benzeneHCID 2234495729.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 4-(4-methoxy-phenoxy)-3,5-dichloro-nitrobenzene (1 g, 3.4 mmol), p-fluorophenylsulfonyl chloride (1.33 g, 6.8 mmol) and Eaton's reagent (20 mL) was stirred at 110° C. for 4.5 h and the solution turned brown. The brown solution was poured into ice water and extracted with EtOAc (3×30 mL). The combined extracts were washed with sat'd sodium bicarbonate (3×50 mL), brine (50 mL), dried and concentrated. The residue was purified by chromatography (20% EtOAc in Hexanes) to give the title compound of Step A (468 mg). MS (APCl−) Calc.: 471.0, Found: 470.0 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664291B2
Source datasetuspto-grants-2003_12
ORD IDord-6c2d0b7d461e49f798f6544de2eadc69
Source noteuspto-grants-2003_12