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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782295Generated: October 30, 2026

Hydrochloric Acid → 6-Chloro-5-(trifluoromethyl)pyridine-3-sulfonyl chloride

https://huagongshe.com/reaction/1782295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
Reactant6-Chloro-5-(trifluoromethyl)pyridin-3-amineHCID 13532244—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product6-Chloro-5-(trifluoromethyl)pyridine-3-sulfonyl chlorideHCID 7070072727%

Reaction Steps

Under ice-cooling, thionyl chloride (4 mL) was added dropwise over 20 min to water (27 mL). The mixture was stirred at room temperature for 12 hr to give a sulfur dioxide-containing solution. Separately, 6-chloro-5-(trifluoromethyl)pyridine-3-amine (1.14 g) was added to concentrated hydrochloric acid (9 mL) with stirring under ice-cooling, and concentrated hydrochloric acid (9 mL) was further added. A solution of sodium nitrite (0.44 g) in water (6 mL) was added dropwise over 10 min. The reaction mixture was gradually added at 5° C. to the above-mentioned sulfur dioxide-containing solution added with cuprous chloride (15 mg). Under ice-cooling, the mixture was further stirred for 30 min, and the precipitate was collected by filtration and washed with water. The obtained precipitate was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=19:1→9:1) to give the title compound as an orange solid (yield 437 mg, 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498337B2
Source datasetuspto-grants-2009_03
ORD IDord-fd4e953545234f1ca82bae093906a7d8
Source noteuspto-grants-2009_03