Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957235Generated: October 26, 2026

Hydrochloric Acid → 3-Chloro-2-(4-chloro-3-methoxyphenyl)-5-trifluoromethylpyridine

https://huagongshe.com/reaction/1957235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,3-Dichloro-5-(trifluoromethyl)pyridineHCID 112234—
ReactantSodium BicarbonateHCID 516892—
Reactant(4-Chloro-3-methoxyphenyl)boronic acidHCID 23005377—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-Chloro-2-(4-chloro-3-methoxyphenyl)-5-trifluoromethylpyridineHCID 15766876—

Reaction Steps

38.8 g (0.180 mol) of 2,3-dichloro-5-trifluoromethylpyridine, 33.5 g (0.180 mol) of 4-chloro-3-methoxybenzeneboronic acid, 0.7 g (0.61 mmol) of tetrakis(triphenylphosphine)palladium(O) and 45.3 g (0.539 mol) of sodium bicarbonate in a mixture of 550 ml of dimethoxyethane and 550 ml of water were refluxed for four hours. The mixture was then acidified to pH 4-5 with dilute hydrochloric acid, the dimethoxyethane was removed by distillation, and the remaining aqueous phase was extracted with methylene chloride. The combined methylene chloride phases were washed with water, dried over sodium sulfate and evaporated. The residue was stirred with a little cold n-hexane, filtered off with suction and dried. Yield: 44.2 g (76%) of colorless crystals of melting point 72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783522
Source datasetuspto-grants-1998_07
ORD IDord-8b8f5deeef36419ba21a77359e60fb53
Source noteuspto-grants-1998_07