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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069502Generated: November 1, 2026

Hydrochloric Acid → 2-Chloro-5-pyridinesulfonyl chloride

https://huagongshe.com/reaction/2069502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
Reactant5-Amino-2-chloropyridineHCID 79305—
ReactantSodium NitriteHCID 23668193—
CatalystCupric chloride dihydrateHCID 61482—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2-Chloro-5-pyridinesulfonyl chlorideHCID 2792792—

Reaction Steps

A solution of 10 g (79.2 mmol) of 3-amino-6-chloropyridine in concentrated HCl (16 mL) and glacial acetic acid (89 mL) was cooled to 10° C. in an ice batch. 5.46 g (79.2 mmol) of sodium nitrite were added portionwise keeping the temperature below 15° C. The mixture was stirred for 1 h, then added dropwise to a solution of sulfur dioxide (ca. 27 mL), 2.77 g (16.2 mmol) of copper (II) chloride dihydrate and acetic acid (59 mL) in water (11 mL) over 10 min at 5° C. The reaction mixture was allowed to warm to room temperature and poured over ice/water (300 mL) and stirred for a further 15 min The resultant precipitate was isolated by filtration, washed with water (2×100 mL) and dried under reduced pressure to afford 12.99 g of 6-chloro-pyridine-3-sulfonyl chloride; 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.62 (1 H, d, J=8.31 Hz), 8.26 (1 H, dd, J=8.56, 2.69 Hz), 9.04 (1 H, d, J=2.69 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299111B2
Source datasetuspto-grants-2012_10
ORD IDord-d1a8f4c8ac5741c298f4e41c59c1f3dc
Source noteuspto-grants-2012_10