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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401755Generated: October 27, 2026

Hydrochloric Acid → Methyl 3-chloro-4-(chlorosulfonyl)benzoate

https://huagongshe.com/reaction/401755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
ReactantMethyl 4-Amino-3-chlorobenzoateHCID 1515284—
ReactantSodium NitriteHCID 23668193—
CatalystCuprous chlorideHCID 62652—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductMethyl 3-chloro-4-(chlorosulfonyl)benzoateHCID 4700298850%

Reaction Steps

To a suspension of methyl 4-amino-3-chlorobenzoate (33 g, 146 mmol, 1 eq) in a 1:1 mixture of concentrated HCl and water (140 ml) cooling in an ice/MeOH bath was added a solution of sodium nitrite (11.1 g, 160 mmol, 1.1 eq) in warm water (20 ml) dropwise, ensuring that the reaction temperature was maintained below 5° C. The mixture was filtered through a pad of Celite and the solids washed with water. The resulting filtrate was added portionwise to a mixture of sulphur dioxide (47 g, 729 mmol, 5 eq) and copper (I) chloride (catalytic) in AcOH, maintaining the reaction temperature below 10° C. The reaction mixture was extracted into DCM (600 ml), washed with water (600 ml), dried over sodium sulphate, filtered and the solvent evaporated in vacuo. The residue was redissolved in DCM, washed with saturated sodium hydrogen carbonate, dried over sodium sulphate, filtered and evaporated in vacuo. The crude material was purified by column chromatography eluting with 0-15% ethyl acetate:hexane then triturated with hexane to yield the title compound (19.6 g, 73.6 mmol, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741934B2
Source datasetuspto-grants-2014_06
ORD IDord-a0fae7c029db4f88a99ddee158663abe
Source noteuspto-grants-2014_06