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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401760Generated: October 26, 2026

Hydrochloric Acid → Methyl 4-(chlorosulfonyl)-2-fluorobenzoate

https://huagongshe.com/reaction/401760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
ReactantSodium NitriteHCID 23668193—
ReactantMethyl 4-amino-2-fluorobenzoate hydrochlorideHCID 68517562—
CatalystCuprous chlorideHCID 62652—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
ProductMethyl 4-(chlorosulfonyl)-2-fluorobenzoateHCID 5773214650,649.398%

Reaction Steps

To a suspension of methyl 4-amino-2-fluorobenzoate hydrochloride (Preparation 12, 33.2 g, 0.154 mmol, 1 eq) in a 1:1 mixture of concentrated HCl and water (70 ml:70 ml) cooling in an ice bath was added a solution of sodium nitrite (11.71 g, 0.169 mol, 1.1 eq) in warm water (20 ml) dropwise maintaining the temperature below 50° C. The reaction mixture was allowed to stir for 10 minutes then filtered through a pad of Celite and the solid washed with water. The filtrate was added portionwise to a solution of sulphur dioxide (49.4 g, 0.771 mmol, 5 eq) and copper (1) chloride (100 mg) in AcOH (120 ml) at 0° C. and the reaction mixture stirred for 30 minutes. The mixture was extracted with DCM (3×150 ml), washed with saturated sodium hydrogen carbonate, water and brine, dried over magnesium sulphate, filtered and evaporated in vacuo. The crude material was purified by column chromatography eluting with 10% ethyl acetate:hexane to yield the title compound as a red oil (19.68 g, 0.078 mol, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741934B2
Source datasetuspto-grants-2014_06
ORD IDord-161e331dc42b47189ff86387c76b1b62
Source noteuspto-grants-2014_06