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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231900Generated: October 25, 2026

Hydrochloric Acid → 4-Chloro-5-(4-chlorophenoxy)-2-nitrobenzoic Acid

https://huagongshe.com/reaction/231900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-ChlorophenolHCID 4684—
ReactantSodium hydrideHCID 24758—
Reactant4,5-Dichloro-2-nitrobenzoic acidHCID 583642—
SolventDiglymeHCID 8150—
Product4-Chloro-5-(4-chlorophenoxy)-2-nitrobenzoic AcidHCID 14233424—

Reaction Conditions

Temperature10 °C

Reaction Steps

To 30 ml of dry diglyme under a nitrogen atmosphere was added 0.960 g (0.02 mol) cf sodium hydride dispersion in mineral oil (50%). The solution was cooled to 10° C. and 1.28 g (0.01M) 4-chlorophenol in 15 ml of dry diglyme was added dropwise while maintaining the temperature at 10° C. This was followed by the dropwise addition of 2.36 g (0.01 mol) of 4,5-dichloro-2-nitrobenzoic acid in 15 ml of dry diglyme. The reaction mixture was then heated to 153° C. (oil bath) for 1 hour and 45 minutes. The reaction mixture was cooled to room temperature and poured into an ice/water mixture. The pH was then adjusted to 1.5 with 6N hydrochloric acid. The solution was extracted with ethyl acetate, and the organic layer dried over anhydrous magnesium sulfate. The solvent was removed and the crude solid triturated with hexane, followed by recrystallization from carbon tetrachloride to give the title compound: yield 1.65 g (50%) m.p. 160°-162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04849518
Source datasetuspto-grants-1989_07
ORD IDord-81bc965b63994068b5b85b7bcbce073c
Source noteuspto-grants-1989_07