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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846335Generated: October 31, 2026

Hydrochloric Acid → 2,3-Difluoro-6-nitro-(2-p-toluenesulfonyloxypropyl)oxybenzene

https://huagongshe.com/reaction/846335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantEthyl AcetateHCID 8857—
Reactant2,3-Difluoro-6-nitro-[(2-hydroxypropyl)oxy]benzeneHCID 14697186—
SolventPyridineHCID 1049—
Product2,3-Difluoro-6-nitro-(2-p-toluenesulfonyloxypropyl)oxybenzeneHCID 1469719487.2%

Reaction Steps

To a solution of 4.5 g of the compound obtained in Example 5 in 8.6 ml of pyridine was added 4.36 g of p-toluenesulfonyl chloride and the mixture was stirred under cooling with ice for 4 hours, and then at room temperature for 4 hours. To the mixture were added ethyl acetate and 1 N hydrochloric acid. The mixture was shaken, and the organic layer was separated. The organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified through silica gel column chromatography to yield 6.52 g of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05136059
Source datasetuspto-grants-1992_08
ORD IDord-c9befeeaef754feabada5e183d0022f7
Source noteuspto-grants-1992_08