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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325052Generated: October 26, 2026

Water → 2-Chloro-4-fluorobenzenesulfonic acid, 3-[2-(4-cyanophenyl)ethoxy]-5-chlorophenyl ester

https://huagongshe.com/reaction/325052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Chloro-4-fluorobenzene-1-sulfonyl chlorideHCID 522846—
Reactant3-Chloro-5-[2-(4-cyanophenyl)ethoxy]phenolHCID 22033534—
SolventPyridineHCID 1049—
Product2-Chloro-4-fluorobenzenesulfonic acid, 3-[2-(4-cyanophenyl)ethoxy]-5-chlorophenyl esterHCID 5728254972.1%

Reaction Steps

2-Chloro-4-fluorobenzenesulfonyl chloride (1.16 g; 5.0 mmol) was added to a cold solution (ice:water temperature) of 3-chloro-5-[2-(4-cyanophenyl)-ethoxy]phenol (0.689 g; 2.5 mmol; from step (ii) above) in pyridine (8 mL). The temperature was allowed to rise (slowly) to ambient overnight. The mixture was re-cooled (ice:water temperature) and ice was added to the reaction flask. After stirring for 4 hours, the pyridine was removed in vacuo. CH2Cl2 was then added and the organic layer was washed with aqueous KHSO4 and water. Drying (MgSO4), evaporation of the solvent and purification by flash chromatography (SiO2; CH2Cl2) afforded 0.84 g (72%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06221898B1
Source datasetuspto-grants-2001_04
ORD IDord-c1f1c3cb484f4767b80e35c1d18b489a
Source noteuspto-grants-2001_04