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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325043Generated: October 30, 2026

2-Chlorobenzenesulfonyl chloride → HCID 86584800, compound

https://huagongshe.com/reaction/325043

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzenesulfonyl chlorideHCID 76187—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86584801HCID 86584801—
SolventPyridineHCID 1049—
ProductHCID 86584800HCID 8658480062%

Reaction Steps

2-Chlorobenzenesulfonyl chloride (0.225 g; 1.06 mmol) was added to a cold solution (ice:water temperature) of 3-[2-(4-cyanophenyl)ethoxy]-5-methyl-phenylaminoacetic acid, ethyl ester (0.30 g; 0.88 mmol; from step (i) above) in pyridine (10 mL). After 2 hours stirring the temperature was allowed to rise to ambient. After 4 hours at this temperature more 2-chloro-benzenesulfonyl chloride (0.056 g; 0.26 mmol) was added and the mixture was left overnight. The mixture was then poured into aqueous saturated NaHCO3 and extracted twice with Et2O. The combined ether phases where washed with HCl/aq (2M), H2O and brine, dried (MgSO4) and the solvent removed in vacuo. The residue was purified by flash chromatography (SiO2; EtOAc:heptane (1:3)) to give 0.28 g (62%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06221898B1
Source datasetuspto-grants-2001_04
ORD IDord-0b7a0c4e7c8147acb4d8af2c92ba8d43
Source noteuspto-grants-2001_04